{"pvalue":0.375,"sign":-1,"group":"AB1: Infectious diseases","label":"Actinomycosis","text":"Phenotype: Actinomycosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.375<br>N cases: 93<br>N controls: 332343"}
{"pvalue":0.0506,"sign":1,"group":"AB1: Infectious diseases","label":"Amoebiasis","text":"Phenotype: Amoebiasis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0506<br>N cases: 149<br>N controls: 336396"}
{"pvalue":0.112,"sign":1,"group":"AB1: Infectious diseases","label":"Anogenital herpesviral [herpes simplex] infection","text":"Phenotype: Anogenital herpesviral [herpes simplex] infection<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.112<br>N cases: 1812<br>N controls: 366340"}
{"pvalue":0.287,"sign":-1,"group":"AB1: Infectious diseases","label":"Aspergillosis","text":"Phenotype: Aspergillosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.287<br>N cases: 194<br>N controls: 369098"}
{"pvalue":0.0352,"sign":-1,"group":"AB1: Infectious diseases","label":"Atypical virus infections of central nervous system","text":"Phenotype: Atypical virus infections of central nervous system<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0352<br>N cases: 260<br>N controls: 375157"}
{"pvalue":0.0113,"sign":1,"group":"AB1: Infectious diseases","label":"Bacterial, viral and other infectious agents","text":"Phenotype: Bacterial, viral and other infectious agents<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0113<br>N cases: 2591<br>N controls: 374686"}
{"pvalue":0.0157,"sign":-1,"group":"AB1: Infectious diseases","label":"Bacterial infection, other or unspecified","text":"Phenotype: Bacterial infection, other or unspecified<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0157<br>N cases: 18576<br>N controls: 332343"}
{"pvalue":0.656,"sign":1,"group":"AB1: Infectious diseases","label":"Other bacterial intestinal infections","text":"Phenotype: Other bacterial intestinal infections<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.656<br>N cases: 5631<br>N controls: 336396"}
{"pvalue":0.606,"sign":-1,"group":"AB1: Infectious diseases","label":"Candidiasis","text":"Phenotype: Candidiasis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.606<br>N cases: 3974<br>N controls: 369098"}
{"pvalue":0.697,"sign":-1,"group":"AB1: Infectious diseases","label":"Other sexually transmitted chlamydial diseases","text":"Phenotype: Other sexually transmitted chlamydial diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.697<br>N cases: 2011<br>N controls: 366340"}
{"pvalue":0.0636,"sign":1,"group":"AB1: Infectious diseases","label":"Cholera","text":"Phenotype: Cholera<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0636<br>N cases: 1290<br>N controls: 336396"}
{"pvalue":0.425,"sign":-1,"group":"AB1: Infectious diseases","label":"Dermatophytosis","text":"Phenotype: Dermatophytosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.425<br>N cases: 3554<br>N controls: 369098"}
{"pvalue":0.0693,"sign":1,"group":"AB1: Infectious diseases","label":"Early syphilis","text":"Phenotype: Early syphilis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0693<br>N cases: 286<br>N controls: 366340"}
{"pvalue":0.35,"sign":1,"group":"AB1: Infectious diseases","label":"Infectious mononucleosis","text":"Phenotype: Infectious mononucleosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.35<br>N cases: 2353<br>N controls: 367472"}
{"pvalue":0.396,"sign":-1,"group":"AB1: Infectious diseases","label":"Enterobiasis","text":"Phenotype: Enterobiasis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.396<br>N cases: 98<br>N controls: 376807"}
{"pvalue":0.518,"sign":1,"group":"AB1: Infectious diseases","label":"Erysipelas","text":"Phenotype: Erysipelas<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.518<br>N cases: 20470<br>N controls: 332343"}
{"pvalue":0.717,"sign":-1,"group":"AB1: Infectious diseases","label":"Diarrhoea and gastroenteritis of presumed infectious origin","text":"Phenotype: Diarrhoea and gastroenteritis of presumed infectious origin<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.717<br>N cases: 29401<br>N controls: 336396"}
{"pvalue":0.319,"sign":-1,"group":"AB1: Infectious diseases","label":"Gonococcal infection","text":"Phenotype: Gonococcal infection<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.319<br>N cases: 878<br>N controls: 366340"}
{"pvalue":0.972,"sign":-1,"group":"AB1: Infectious diseases","label":"Helminthiases","text":"Phenotype: Helminthiases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.972<br>N cases: 470<br>N controls: 376807"}
{"pvalue":0.275,"sign":-1,"group":"AB1: Infectious diseases","label":"Acute hepatitis A","text":"Phenotype: Acute hepatitis A<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.275<br>N cases: 118<br>N controls: 375134"}
{"pvalue":0.184,"sign":1,"group":"AB1: Infectious diseases","label":"Acute hepatitis B","text":"Phenotype: Acute hepatitis B<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.184<br>N cases: 110<br>N controls: 375134"}
{"pvalue":0.136,"sign":1,"group":"AB1: Infectious diseases","label":"Herpesviral [herpes simplex] infections","text":"Phenotype: Herpesviral [herpes simplex] infections<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.136<br>N cases: 3374<br>N controls: 362997"}
{"pvalue":0.168,"sign":1,"group":"AB1: Infectious diseases","label":"Unspecified human immunodeficiency virus [HIV] disease","text":"Phenotype: Unspecified human immunodeficiency virus [HIV] disease<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.168<br>N cases: 245<br>N controls: 376773"}
{"pvalue":0.755,"sign":-1,"group":"AB1: Infectious diseases","label":"Intestinal infectious diseases","text":"Phenotype: Intestinal infectious diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.755<br>N cases: 40881<br>N controls: 336396"}
{"pvalue":0.503,"sign":-1,"group":"AB1: Infectious diseases","label":"Late syphilis","text":"Phenotype: Late syphilis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.503<br>N cases: 347<br>N controls: 366340"}
{"pvalue":0.342,"sign":1,"group":"AB1: Infectious diseases","label":"Listeriosis","text":"Phenotype: Listeriosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.342<br>N cases: 117<br>N controls: 332343"}
{"pvalue":0.29,"sign":-1,"group":"AB1: Infectious diseases","label":"Malaria","text":"Phenotype: Malaria<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.29<br>N cases: 129<br>N controls: 376614"}
{"pvalue":0.119,"sign":-1,"group":"AB1: Infectious diseases","label":"Measles","text":"Phenotype: Measles<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.119<br>N cases: 319<br>N controls: 362997"}
{"pvalue":0.499,"sign":-1,"group":"AB1: Infectious diseases","label":"Meningococcal infection","text":"Phenotype: Meningococcal infection<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.499<br>N cases: 215<br>N controls: 332343"}
{"pvalue":0.386,"sign":1,"group":"AB1: Infectious diseases","label":"Mumps","text":"Phenotype: Mumps<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.386<br>N cases: 744<br>N controls: 367472"}
{"pvalue":0.388,"sign":-1,"group":"AB1: Infectious diseases","label":"Mycoses","text":"Phenotype: Mycoses<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.388<br>N cases: 8179<br>N controls: 369098"}
{"pvalue":0.388,"sign":-1,"group":"AB1: Infectious diseases","label":"Other bacterial diseases","text":"Phenotype: Other bacterial diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.388<br>N cases: 44934<br>N controls: 332343"}
{"pvalue":0.742,"sign":-1,"group":"AB1: Infectious diseases","label":"Other bacterial agents as the cause of diseases classified to other chapters","text":"Phenotype: Other bacterial agents as the cause of diseases classified to other chapters<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.742<br>N cases: 259<br>N controls: 374686"}
{"pvalue":0.602,"sign":-1,"group":"AB1: Infectious diseases","label":"Other cestode infections","text":"Phenotype: Other cestode infections<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.602<br>N cases: 94<br>N controls: 376807"}
{"pvalue":0.387,"sign":1,"group":"AB1: Infectious diseases","label":"Other diseases caused by chlamydiae","text":"Phenotype: Other diseases caused by chlamydiae<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.387<br>N cases: 314<br>N controls: 376963"}
{"pvalue":0.238,"sign":1,"group":"AB1: Infectious diseases","label":"Human immunodeficiency virus [HIV] disease resulting in other conditions","text":"Phenotype: Human immunodeficiency virus [HIV] disease resulting in other conditions<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.238<br>N cases: 459<br>N controls: 376773"}
{"pvalue":0.924,"sign":-1,"group":"AB1: Infectious diseases","label":"Other infectious diseases","text":"Phenotype: Other infectious diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.924<br>N cases: 2347<br>N controls: 374930"}
{"pvalue":0.32,"sign":1,"group":"AB1: Infectious diseases","label":"Infection due to other mycobacteria","text":"Phenotype: Infection due to other mycobacteria<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.32<br>N cases: 395<br>N controls: 332343"}
{"pvalue":0.564,"sign":-1,"group":"AB1: Infectious diseases","label":"Other protozoal intestinal diseases","text":"Phenotype: Other protozoal intestinal diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.564<br>N cases: 336<br>N controls: 336396"}
{"pvalue":0.134,"sign":-1,"group":"AB1: Infectious diseases","label":"Other septicaemia","text":"Phenotype: Other septicaemia<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.134<br>N cases: 12301<br>N controls: 332343"}
{"pvalue":0.0404,"sign":1,"group":"AB1: Infectious diseases","label":"Other spirochaetal diseases","text":"Phenotype: Other spirochaetal diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0404<br>N cases: 2292<br>N controls: 374985"}
{"pvalue":0.464,"sign":-1,"group":"AB1: Infectious diseases","label":"Other superficial mycoses","text":"Phenotype: Other superficial mycoses<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.464<br>N cases: 491<br>N controls: 369098"}
{"pvalue":0.99,"sign":1,"group":"AB1: Infectious diseases","label":"Other viral diseases","text":"Phenotype: Other viral diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.99<br>N cases: 9805<br>N controls: 367472"}
{"pvalue":0.218,"sign":1,"group":"AB1: Infectious diseases","label":"Unspecified parasitic disease","text":"Phenotype: Unspecified parasitic disease<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.218<br>N cases: 223<br>N controls: 375759"}
{"pvalue":0.923,"sign":-1,"group":"AB1: Infectious diseases","label":"Pediculosis, acariasis and other infestations","text":"Phenotype: Pediculosis, acariasis and other infestations<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.923<br>N cases: 1518<br>N controls: 375759"}
{"pvalue":0.676,"sign":1,"group":"AB1: Infectious diseases","label":"Pediculosis and phthiriasis","text":"Phenotype: Pediculosis and phthiriasis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.676<br>N cases: 81<br>N controls: 375759"}
{"pvalue":0.958,"sign":-1,"group":"AB1: Infectious diseases","label":"Pneumocystosis","text":"Phenotype: Pneumocystosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.958<br>N cases: 353<br>N controls: 376614"}
{"pvalue":0.0187,"sign":-1,"group":"AB1: Infectious diseases","label":"Acute poliomyelitis","text":"Phenotype: Acute poliomyelitis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0187<br>N cases: 369<br>N controls: 375157"}
{"pvalue":0.688,"sign":-1,"group":"AB1: Infectious diseases","label":"Protozoal diseases","text":"Phenotype: Protozoal diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.688<br>N cases: 663<br>N controls: 376614"}
{"pvalue":0.669,"sign":-1,"group":"AB1: Infectious diseases","label":"Respiratory tuberculosis, bacteriologically and histologically confirmed","text":"Phenotype: Respiratory tuberculosis, bacteriologically and histologically confirmed<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.669<br>N cases: 543<br>N controls: 374845"}
{"pvalue":0.8,"sign":-1,"group":"AB1: Infectious diseases","label":"Respiratory tuberculosis, not confirmed bacteriologically or histologically","text":"Phenotype: Respiratory tuberculosis, not confirmed bacteriologically or histologically<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.8<br>N cases: 1329<br>N controls: 374845"}
{"pvalue":0.565,"sign":1,"group":"AB1: Infectious diseases","label":"Rubella [German measles]","text":"Phenotype: Rubella [German measles]<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.565<br>N cases: 955<br>N controls: 362997"}
{"pvalue":0.597,"sign":-1,"group":"AB1: Infectious diseases","label":"Other salmonella infections","text":"Phenotype: Other salmonella infections<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.597<br>N cases: 1046<br>N controls: 336396"}
{"pvalue":0.248,"sign":-1,"group":"AB1: Infectious diseases","label":"Scabies","text":"Phenotype: Scabies<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.248<br>N cases: 1105<br>N controls: 375759"}
{"pvalue":0.36,"sign":-1,"group":"AB1: Infectious diseases","label":"Scarlet fever","text":"Phenotype: Scarlet fever<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.36<br>N cases: 186<br>N controls: 332343"}
{"pvalue":0.745,"sign":1,"group":"AB1: Infectious diseases","label":"Sequelae of other and unspecified infectious and parasitic diseases","text":"Phenotype: Sequelae of other and unspecified infectious and parasitic diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.745<br>N cases: 1624<br>N controls: 374884"}
{"pvalue":0.486,"sign":-1,"group":"AB1: Infectious diseases","label":"Sequelae of poliomyelitis","text":"Phenotype: Sequelae of poliomyelitis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.486<br>N cases: 204<br>N controls: 374884"}
{"pvalue":0.548,"sign":1,"group":"AB1: Infectious diseases","label":"Sequelae of tuberculosis","text":"Phenotype: Sequelae of tuberculosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.548<br>N cases: 569<br>N controls: 374884"}
{"pvalue":0.664,"sign":1,"group":"AB1: Infectious diseases","label":"Sequelae of infectious and parasitic diseases","text":"Phenotype: Sequelae of infectious and parasitic diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.664<br>N cases: 2393<br>N controls: 374884"}
{"pvalue":0.294,"sign":-1,"group":"AB1: Infectious diseases","label":"Infections with a predominantly sexual mode of transmission","text":"Phenotype: Infections with a predominantly sexual mode of transmission<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.294<br>N cases: 10937<br>N controls: 366340"}
{"pvalue":0.0285,"sign":-1,"group":"AB1: Infectious diseases","label":"Other predominantly sexually transmitted diseases, not elsewhere classified","text":"Phenotype: Other predominantly sexually transmitted diseases, not elsewhere classified<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0285<br>N cases: 5753<br>N controls: 366340"}
{"pvalue":0.302,"sign":-1,"group":"AB1: Infectious diseases","label":"Shigellosis","text":"Phenotype: Shigellosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.302<br>N cases: 83<br>N controls: 336396"}
{"pvalue":0.75,"sign":-1,"group":"AB1: Infectious diseases","label":"Streptococcal septicaemia","text":"Phenotype: Streptococcal septicaemia<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.75<br>N cases: 2348<br>N controls: 332343"}
{"pvalue":0.866,"sign":-1,"group":"AB1: Infectious diseases","label":"Streptococcus and staphylococcus as the cause of diseases classified to other chapters","text":"Phenotype: Streptococcus and staphylococcus as the cause of diseases classified to other chapters<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.866<br>N cases: 151<br>N controls: 374686"}
{"pvalue":0.552,"sign":1,"group":"AB1: Infectious diseases","label":"Syphilis","text":"Phenotype: Syphilis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.552<br>N cases: 662<br>N controls: 366340"}
{"pvalue":0.296,"sign":-1,"group":"AB1: Infectious diseases","label":"Tick-borne viral encephalitis","text":"Phenotype: Tick-borne viral encephalitis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.296<br>N cases: 82<br>N controls: 375157"}
{"pvalue":0.877,"sign":1,"group":"AB1: Infectious diseases","label":"Toxoplasmosis","text":"Phenotype: Toxoplasmosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.877<br>N cases: 154<br>N controls: 376614"}
{"pvalue":0.33,"sign":-1,"group":"AB1: Infectious diseases","label":"Trichomoniasis","text":"Phenotype: Trichomoniasis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.33<br>N cases: 219<br>N controls: 366340"}
{"pvalue":0.712,"sign":-1,"group":"AB1: Infectious diseases","label":"Tuberculosis","text":"Phenotype: Tuberculosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.712<br>N cases: 2432<br>N controls: 374845"}
{"pvalue":0.603,"sign":1,"group":"AB1: Infectious diseases","label":"Tuberculosis of other organs","text":"Phenotype: Tuberculosis of other organs<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.603<br>N cases: 676<br>N controls: 374845"}
{"pvalue":0.829,"sign":-1,"group":"AB1: Infectious diseases","label":"Tularaemia","text":"Phenotype: Tularaemia<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.829<br>N cases: 298<br>N controls: 376827"}
{"pvalue":0.346,"sign":1,"group":"AB1: Infectious diseases","label":"Typhoid and paratyphoid fevers","text":"Phenotype: Typhoid and paratyphoid fevers<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.346<br>N cases: 114<br>N controls: 336396"}
{"pvalue":0.691,"sign":-1,"group":"AB1: Infectious diseases","label":"Varicella [chickenpox]","text":"Phenotype: Varicella [chickenpox]<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.691<br>N cases: 1289<br>N controls: 362997"}
{"pvalue":0.862,"sign":1,"group":"AB1: Infectious diseases","label":"Viral conjunctivitis","text":"Phenotype: Viral conjunctivitis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.862<br>N cases: 556<br>N controls: 367472"}
{"pvalue":0.0153,"sign":-1,"group":"AB1: Infectious diseases","label":"Viral infections of the central nervous system","text":"Phenotype: Viral infections of the central nervous system<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0153<br>N cases: 2120<br>N controls: 375157"}
{"pvalue":0.0338,"sign":-1,"group":"AB1: Infectious diseases","label":"Viral encephalitis, not elsewhere classified/unspecified","text":"Phenotype: Viral encephalitis, not elsewhere classified/unspecified<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0338<br>N cases: 536<br>N controls: 375157"}
{"pvalue":0.493,"sign":-1,"group":"AB1: Infectious diseases","label":"Viral haemorrhagic fevers, not elsewhere classified/unspecified","text":"Phenotype: Viral haemorrhagic fevers, not elsewhere classified/unspecified<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.493<br>N cases: 2166<br>N controls: 374565"}
{"pvalue":0.975,"sign":-1,"group":"AB1: Infectious diseases","label":"Viral hepatitis","text":"Phenotype: Viral hepatitis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.975<br>N cases: 2143<br>N controls: 375134"}
{"pvalue":0.995,"sign":1,"group":"AB1: Infectious diseases","label":"Viral agents as the cause of diseases classified to other chapters","text":"Phenotype: Viral agents as the cause of diseases classified to other chapters<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.995<br>N cases: 535<br>N controls: 374686"}
{"pvalue":0.128,"sign":-1,"group":"AB1: Infectious diseases","label":"Viral meningitis","text":"Phenotype: Viral meningitis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.128<br>N cases: 1012<br>N controls: 375157"}
{"pvalue":0.431,"sign":-1,"group":"AB1: Infectious diseases","label":"Other viral diseases, not elsewhere classified","text":"Phenotype: Other viral diseases, not elsewhere classified<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.431<br>N cases: 5864<br>N controls: 367472"}
{"pvalue":0.0564,"sign":-1,"group":"AB1: Infectious diseases","label":"Viral and other specified intestinal infections","text":"Phenotype: Viral and other specified intestinal infections<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0564<br>N cases: 7613<br>N controls: 336396"}
{"pvalue":0.161,"sign":1,"group":"AB1: Infectious diseases","label":"Viral infections characterized by skin and mucous membrane lesions","text":"Phenotype: Viral infections characterized by skin and mucous membrane lesions<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.161<br>N cases: 14280<br>N controls: 362997"}
{"pvalue":0.716,"sign":-1,"group":"AB1: Infectious diseases","label":"Other viral infections characterized by skin and mucous membrane lesions, not elsewhere classified","text":"Phenotype: Other viral infections characterized by skin and mucous membrane lesions, not elsewhere classified<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.716<br>N cases: 1009<br>N controls: 362997"}
{"pvalue":0.278,"sign":1,"group":"AB1: Infectious diseases","label":"Viral warts","text":"Phenotype: Viral warts<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.278<br>N cases: 2940<br>N controls: 362997"}
{"pvalue":0.627,"sign":-1,"group":"AB1: Infectious diseases","label":"Viral infections of central nervous system, not elsewhere classified/unspecified","text":"Phenotype: Viral infections of central nervous system, not elsewhere classified/unspecified<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.627<br>N cases: 310<br>N controls: 375157"}
{"pvalue":0.144,"sign":1,"group":"AB1: Infectious diseases","label":"Whooping cough","text":"Phenotype: Whooping cough<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.144<br>N cases: 147<br>N controls: 332343"}
{"pvalue":0.896,"sign":1,"group":"AB1: Infectious diseases","label":"Certain zoonotic bacterial diseases","text":"Phenotype: Certain zoonotic bacterial diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.896<br>N cases: 450<br>N controls: 376827"}
{"pvalue":0.427,"sign":1,"group":"AB1: Infectious diseases","label":"Zoster [herpes zoster]","text":"Phenotype: Zoster [herpes zoster]<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.427<br>N cases: 4973<br>N controls: 362997"}
{"pvalue":0.0186,"sign":1,"group":"K11: Digestive system diseases","label":"Hernia of abdominal wall","text":"Phenotype: Hernia of abdominal wall<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0186<br>N cases: 15338<br>N controls: 361939"}
{"pvalue":0.484,"sign":1,"group":"K11: Digestive system diseases","label":"Hernia of abdominal wall, postoperative","text":"Phenotype: Hernia of abdominal wall, postoperative<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.484<br>N cases: 5775<br>N controls: 210314"}
{"pvalue":0.344,"sign":1,"group":"J10: Respiratory system diseases","label":"Acute drug-induced interstitial lung disorder","text":"Phenotype: Acute drug-induced interstitial lung disorder<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.344<br>N cases: 192<br>N controls: 377085"}
{"pvalue":0.755,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Alcohol withdrawal state with delirium ","text":"Phenotype: Alcohol withdrawal state with delirium <br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.755<br>N cases: 2058<br>N controls: 375219"}
{"pvalue":0.373,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Allergic contact dermatitis due to drugs in contact with skin","text":"Phenotype: Allergic contact dermatitis due to drugs in contact with skin<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.373<br>N cases: 574<br>N controls: 376703"}
{"pvalue":0.625,"sign":-1,"group":"K11: Digestive system diseases","label":"Acute appendicitis, with complications","text":"Phenotype: Acute appendicitis, with complications<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.625<br>N cases: 6747<br>N controls: 346283"}
{"pvalue":0.0172,"sign":1,"group":"K11: Digestive system diseases","label":"Acute appendicitis, no complications","text":"Phenotype: Acute appendicitis, no complications<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0172<br>N cases: 21998<br>N controls: 346283"}
{"pvalue":0.279,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Alcohol use disorder, ICD-based","text":"Phenotype: Alcohol use disorder, ICD-based<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.279<br>N cases: 15715<br>N controls: 361562"}
{"pvalue":0.69,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Autoimmune hyperthyroidism","text":"Phenotype: Autoimmune hyperthyroidism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.69<br>N cases: 1828<br>N controls: 279855"}
{"pvalue":0.745,"sign":1,"group":"AB1: Infectious diseases","label":"Other specified/unspecified bacterial intestinal infections","text":"Phenotype: Other specified/unspecified bacterial intestinal infections<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.745<br>N cases: 1749<br>N controls: 371656"}
{"pvalue":0.122,"sign":1,"group":"AB1: Infectious diseases","label":"Campylobacter enteritis","text":"Phenotype: Campylobacter enteritis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.122<br>N cases: 701<br>N controls: 371656"}
{"pvalue":0.883,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Adrenal gland","text":"Phenotype: Benign neoplasm: Adrenal gland<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.883<br>N cases: 1790<br>N controls: 375487"}
{"pvalue":0.885,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Anus and anal canal","text":"Phenotype: Benign neoplasm: Anus and anal canal<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.885<br>N cases: 726<br>N controls: 376551"}
{"pvalue":0.641,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Appendix","text":"Phenotype: Benign neoplasm: Appendix<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.641<br>N cases: 251<br>N controls: 377026"}
{"pvalue":0.55,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Ascending colon","text":"Phenotype: Benign neoplasm: Ascending colon<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.55<br>N cases: 3177<br>N controls: 374100"}
{"pvalue":0.705,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Bladder","text":"Phenotype: Benign neoplasm: Bladder<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.705<br>N cases: 239<br>N controls: 377038"}
{"pvalue":0.572,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm of bone and articular cartilage","text":"Phenotype: Benign neoplasm of bone and articular cartilage<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.572<br>N cases: 2335<br>N controls: 374942"}
{"pvalue":0.71,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Bone and articular cartilage, unspecified","text":"Phenotype: Benign neoplasm: Bone and articular cartilage, unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.71<br>N cases: 192<br>N controls: 377085"}
{"pvalue":0.496,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Long bones of lower limb","text":"Phenotype: Benign neoplasm: Long bones of lower limb<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.496<br>N cases: 837<br>N controls: 376440"}
{"pvalue":0.246,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Lower jaw bone","text":"Phenotype: Benign neoplasm: Lower jaw bone<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.246<br>N cases: 114<br>N controls: 377163"}
{"pvalue":0.0275,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Scapula and long bones of upper limb","text":"Phenotype: Benign neoplasm: Scapula and long bones of upper limb<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0275<br>N cases: 254<br>N controls: 377023"}
{"pvalue":0.662,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Short bones of lower limb","text":"Phenotype: Benign neoplasm: Short bones of lower limb<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.662<br>N cases: 262<br>N controls: 377015"}
{"pvalue":0.372,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Short bones of upper limb","text":"Phenotype: Benign neoplasm: Short bones of upper limb<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.372<br>N cases: 397<br>N controls: 376880"}
{"pvalue":0.0764,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Bones of skull and face","text":"Phenotype: Benign neoplasm: Bones of skull and face<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0764<br>N cases: 234<br>N controls: 377043"}
{"pvalue":0.155,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of brain and other parts of central nervous system","text":"Phenotype: Benign neoplasm of brain and other parts of central nervous system<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.155<br>N cases: 1751<br>N controls: 375526"}
{"pvalue":0.767,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Brain, infratentorial","text":"Phenotype: Benign neoplasm: Brain, infratentorial<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.767<br>N cases: 145<br>N controls: 377132"}
{"pvalue":0.828,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Brain, unspecified","text":"Phenotype: Benign neoplasm: Brain, unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.828<br>N cases: 157<br>N controls: 377120"}
{"pvalue":0.3,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Brain, supratentorial","text":"Phenotype: Benign neoplasm: Brain, supratentorial<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.3<br>N cases: 419<br>N controls: 376858"}
{"pvalue":0.884,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of breast","text":"Phenotype: Benign neoplasm of breast<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.884<br>N cases: 3574<br>N controls: 207296"}
{"pvalue":0.127,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Bronchus and lung","text":"Phenotype: Benign neoplasm: Bronchus and lung<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.127<br>N cases: 331<br>N controls: 376946"}
{"pvalue":0.247,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Caecum","text":"Phenotype: Benign neoplasm: Caecum<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.247<br>N cases: 2463<br>N controls: 374814"}
{"pvalue":0.226,"sign":-1,"group":"CD2: Neoplasms","label":"Other benign neoplasm of uterus: Cervix uteri","text":"Phenotype: Other benign neoplasm of uterus: Cervix uteri<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.226<br>N cases: 146<br>N controls: 210724"}
{"pvalue":0.61,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Choroid","text":"Phenotype: Benign neoplasm: Choroid<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.61<br>N cases: 1324<br>N controls: 375953"}
{"pvalue":0.867,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Central nervous system, other parts/unspecified","text":"Phenotype: Benign neoplasm: Central nervous system, other parts/unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.867<br>N cases: 90<br>N controls: 377187"}
{"pvalue":0.18,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Colon","text":"Phenotype: Benign neoplasm: Colon<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.18<br>N cases: 16445<br>N controls: 360832"}
{"pvalue":0.75,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Colon, unspecified","text":"Phenotype: Benign neoplasm: Colon, unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.75<br>N cases: 7013<br>N controls: 370264"}
{"pvalue":0.554,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm of colon, rectum, anus and anal canal","text":"Phenotype: Benign neoplasm of colon, rectum, anus and anal canal<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.554<br>N cases: 20336<br>N controls: 356941"}
{"pvalue":0.236,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Conjunctiva","text":"Phenotype: Benign neoplasm: Conjunctiva<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.236<br>N cases: 824<br>N controls: 376453"}
{"pvalue":0.638,"sign":-1,"group":"CD2: Neoplasms","label":"Other benign neoplasms of connective and other soft tissue","text":"Phenotype: Other benign neoplasms of connective and other soft tissue<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.638<br>N cases: 2857<br>N controls: 374420"}
{"pvalue":0.865,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Connective and other soft tissue of thorax","text":"Phenotype: Benign neoplasm: Connective and other soft tissue of thorax<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.865<br>N cases: 115<br>N controls: 377162"}
{"pvalue":0.62,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Connective and other soft tissue of trunk, unspecified","text":"Phenotype: Benign neoplasm: Connective and other soft tissue of trunk, unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.62<br>N cases: 163<br>N controls: 377114"}
{"pvalue":0.641,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Connective and other soft tissue of upper limb, including shoulder","text":"Phenotype: Benign neoplasm: Connective and other soft tissue of upper limb, including shoulder<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.641<br>N cases: 1156<br>N controls: 376121"}
{"pvalue":0.736,"sign":1,"group":"CD2: Neoplasms","label":"Other benign neoplasm of uterus: Corpus uteri","text":"Phenotype: Other benign neoplasm of uterus: Corpus uteri<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.736<br>N cases: 177<br>N controls: 210693"}
{"pvalue":0.328,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Cranial nerves","text":"Phenotype: Benign neoplasm: Cranial nerves<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.328<br>N cases: 710<br>N controls: 376567"}
{"pvalue":0.206,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Descending colon","text":"Phenotype: Benign neoplasm: Descending colon<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.206<br>N cases: 1571<br>N controls: 375706"}
{"pvalue":0.692,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Ill-defined sites within the digestive system","text":"Phenotype: Benign neoplasm: Ill-defined sites within the digestive system<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.692<br>N cases: 146<br>N controls: 377131"}
{"pvalue":0.983,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Duodenum","text":"Phenotype: Benign neoplasm: Duodenum<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.983<br>N cases: 627<br>N controls: 376650"}
{"pvalue":0.0556,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Middle ear, nasal cavity and accessory sinuses","text":"Phenotype: Benign neoplasm: Middle ear, nasal cavity and accessory sinuses<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0556<br>N cases: 1046<br>N controls: 376231"}
{"pvalue":0.341,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm of middle ear and respiratory system","text":"Phenotype: Benign neoplasm of middle ear and respiratory system<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.341<br>N cases: 2271<br>N controls: 375006"}
{"pvalue":0.336,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Endocrine gland, other/unspecified","text":"Phenotype: Benign neoplasm: Endocrine gland, other/unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.336<br>N cases: 93<br>N controls: 377184"}
{"pvalue":0.243,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of other and unspecified endocrine glands","text":"Phenotype: Benign neoplasm of other and unspecified endocrine glands<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.243<br>N cases: 3544<br>N controls: 373733"}
{"pvalue":0.508,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Endocrine pancreas","text":"Phenotype: Benign neoplasm: Endocrine pancreas<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.508<br>N cases: 135<br>N controls: 377142"}
{"pvalue":0.384,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Epididymis","text":"Phenotype: Benign neoplasm: Epididymis<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.384<br>N cases: 85<br>N controls: 166322"}
{"pvalue":0.527,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm of eye and adnexa","text":"Phenotype: Benign neoplasm of eye and adnexa<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.527<br>N cases: 2555<br>N controls: 374722"}
{"pvalue":0.789,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of other and unspecified female genital organs","text":"Phenotype: Benign neoplasm of other and unspecified female genital organs<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.789<br>N cases: 1151<br>N controls: 209719"}
{"pvalue":0.274,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Floor of mouth","text":"Phenotype: Benign neoplasm: Floor of mouth<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.274<br>N cases: 91<br>N controls: 377186"}
{"pvalue":0.0657,"sign":1,"group":"CD2: Neoplasms","label":"Haemangioma and lymphangioma, any site","text":"Phenotype: Haemangioma and lymphangioma, any site<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0657<br>N cases: 2488<br>N controls: 374789"}
{"pvalue":0.00651,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Heart","text":"Phenotype: Benign neoplasm: Heart<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00651<br>N cases: 81<br>N controls: 377196"}
{"pvalue":0.039,"sign":1,"group":"CD2: Neoplasms","label":"Haemangioma, any site","text":"Phenotype: Haemangioma, any site<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.039<br>N cases: 2292<br>N controls: 374985"}
{"pvalue":0.319,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Hypopharynx","text":"Phenotype: Benign neoplasm: Hypopharynx<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.319<br>N cases: 117<br>N controls: 377160"}
{"pvalue":0.157,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm of other and unspecified intrathoracic organs","text":"Phenotype: Benign neoplasm of other and unspecified intrathoracic organs<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.157<br>N cases: 280<br>N controls: 376997"}
{"pvalue":0.654,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Kidney","text":"Phenotype: Benign neoplasm: Kidney<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.654<br>N cases: 801<br>N controls: 376476"}
{"pvalue":0.337,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Larynx","text":"Phenotype: Benign neoplasm: Larynx<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.337<br>N cases: 887<br>N controls: 376390"}
{"pvalue":0.745,"sign":-1,"group":"CD2: Neoplasms","label":"Leiomyoma of uterus","text":"Phenotype: Leiomyoma of uterus<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.745<br>N cases: 31661<br>N controls: 179209"}
{"pvalue":0.187,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Lip","text":"Phenotype: Benign neoplasm: Lip<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.187<br>N cases: 589<br>N controls: 376688"}
{"pvalue":0.815,"sign":-1,"group":"CD2: Neoplasms","label":"Benign lipomatous neoplasm","text":"Phenotype: Benign lipomatous neoplasm<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.815<br>N cases: 9431<br>N controls: 367846"}
{"pvalue":0.255,"sign":-1,"group":"CD2: Neoplasms","label":"Benign lipomatous neoplasm of other sites/unspecified","text":"Phenotype: Benign lipomatous neoplasm of other sites/unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.255<br>N cases: 2576<br>N controls: 374701"}
{"pvalue":0.772,"sign":1,"group":"CD2: Neoplasms","label":"Benign lipomatous neoplasm of skin and subcutaneous tissue of head, face and neck","text":"Phenotype: Benign lipomatous neoplasm of skin and subcutaneous tissue of head, face and neck<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.772<br>N cases: 1745<br>N controls: 375532"}
{"pvalue":0.613,"sign":-1,"group":"CD2: Neoplasms","label":"Benign lipomatous neoplasm of skin and subcutaneous tissue of limbs","text":"Phenotype: Benign lipomatous neoplasm of skin and subcutaneous tissue of limbs<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.613<br>N cases: 2159<br>N controls: 375118"}
{"pvalue":0.859,"sign":-1,"group":"CD2: Neoplasms","label":"Benign lipomatous neoplasm of skin and subcutaneous tissue of other and unspecified sites","text":"Phenotype: Benign lipomatous neoplasm of skin and subcutaneous tissue of other and unspecified sites<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.859<br>N cases: 183<br>N controls: 377094"}
{"pvalue":0.784,"sign":-1,"group":"CD2: Neoplasms","label":"Benign lipomatous neoplasm of skin and subcutaneous tissue of trunk","text":"Phenotype: Benign lipomatous neoplasm of skin and subcutaneous tissue of trunk<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.784<br>N cases: 3754<br>N controls: 373523"}
{"pvalue":0.952,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Liver/bile ducts","text":"Phenotype: Benign neoplasm: Liver/bile ducts<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.952<br>N cases: 551<br>N controls: 376726"}
{"pvalue":0.875,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Liver","text":"Phenotype: Benign neoplasm: Liver<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.875<br>N cases: 491<br>N controls: 376786"}
{"pvalue":0.644,"sign":-1,"group":"CD2: Neoplasms","label":"Lymphangioma, anys site","text":"Phenotype: Lymphangioma, anys site<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.644<br>N cases: 210<br>N controls: 377067"}
{"pvalue":0.285,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm of male genital organs","text":"Phenotype: Benign neoplasm of male genital organs<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.285<br>N cases: 540<br>N controls: 165867"}
{"pvalue":0.701,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Mediastinum","text":"Phenotype: Benign neoplasm: Mediastinum<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.701<br>N cases: 86<br>N controls: 377191"}
{"pvalue":0.283,"sign":-1,"group":"CD2: Neoplasms","label":"Melanocytic naevi of ear and external auricular canal","text":"Phenotype: Melanocytic naevi of ear and external auricular canal<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.283<br>N cases: 143<br>N controls: 377134"}
{"pvalue":0.765,"sign":1,"group":"CD2: Neoplasms","label":"Melanocytic naevi of eyelid, including canthus","text":"Phenotype: Melanocytic naevi of eyelid, including canthus<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.765<br>N cases: 223<br>N controls: 377054"}
{"pvalue":0.922,"sign":1,"group":"CD2: Neoplasms","label":"Melanocytic naevi of other and unspecified parts of face","text":"Phenotype: Melanocytic naevi of other and unspecified parts of face<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.922<br>N cases: 1574<br>N controls: 375703"}
{"pvalue":0.666,"sign":1,"group":"CD2: Neoplasms","label":"Melanocytic naevi","text":"Phenotype: Melanocytic naevi<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.666<br>N cases: 8900<br>N controls: 368377"}
{"pvalue":0.701,"sign":-1,"group":"CD2: Neoplasms","label":"Melanocytic naevi of lip","text":"Phenotype: Melanocytic naevi of lip<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.701<br>N cases: 224<br>N controls: 377053"}
{"pvalue":0.859,"sign":1,"group":"CD2: Neoplasms","label":"Melanocytic naevi of lower limb, including hip","text":"Phenotype: Melanocytic naevi of lower limb, including hip<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.859<br>N cases: 1108<br>N controls: 376169"}
{"pvalue":0.316,"sign":-1,"group":"CD2: Neoplasms","label":"Melanocytic naevi, other sites/unspecified","text":"Phenotype: Melanocytic naevi, other sites/unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.316<br>N cases: 1992<br>N controls: 375285"}
{"pvalue":0.185,"sign":1,"group":"CD2: Neoplasms","label":"Melanocytic naevi of scalp and neck","text":"Phenotype: Melanocytic naevi of scalp and neck<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.185<br>N cases: 598<br>N controls: 376679"}
{"pvalue":0.788,"sign":-1,"group":"CD2: Neoplasms","label":"Melanocytic naevi of trunk","text":"Phenotype: Melanocytic naevi of trunk<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.788<br>N cases: 3295<br>N controls: 373982"}
{"pvalue":0.555,"sign":-1,"group":"CD2: Neoplasms","label":"Melanocytic naevi of upper limb, including shoulder","text":"Phenotype: Melanocytic naevi of upper limb, including shoulder<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.555<br>N cases: 573<br>N controls: 376704"}
{"pvalue":0.376,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Cerebral meninges","text":"Phenotype: Benign neoplasm: Cerebral meninges<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.376<br>N cases: 2382<br>N controls: 374895"}
{"pvalue":0.412,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of meninges","text":"Phenotype: Benign neoplasm of meninges<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.412<br>N cases: 2655<br>N controls: 374622"}
{"pvalue":0.521,"sign":1,"group":"CD2: Neoplasms","label":"Beningn neoplasm: Meninges, unspecified","text":"Phenotype: Beningn neoplasm: Meninges, unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.521<br>N cases: 400<br>N controls: 376877"}
{"pvalue":0.856,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Spinal meninges","text":"Phenotype: Benign neoplasm: Spinal meninges<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.856<br>N cases: 242<br>N controls: 377035"}
{"pvalue":0.78,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Other and unspecified parts of mouth","text":"Phenotype: Benign neoplasm: Other and unspecified parts of mouth<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.78<br>N cases: 920<br>N controls: 376357"}
{"pvalue":0.682,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of mouth and pharynx","text":"Phenotype: Benign neoplasm of mouth and pharynx<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.682<br>N cases: 3216<br>N controls: 374061"}
{"pvalue":0.279,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Nasopharynx","text":"Phenotype: Benign neoplasm: Nasopharynx<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.279<br>N cases: 224<br>N controls: 377053"}
{"pvalue":0.359,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Other/unspecified site","text":"Phenotype: Benign neoplasm: Other/unspecified site<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.359<br>N cases: 424<br>N controls: 376853"}
{"pvalue":0.682,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Oesophagus","text":"Phenotype: Benign neoplasm: Oesophagus<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.682<br>N cases: 295<br>N controls: 376982"}
{"pvalue":0.685,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Orbit, unspecified","text":"Phenotype: Benign neoplasm: Orbit, unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.685<br>N cases: 150<br>N controls: 377127"}
{"pvalue":0.623,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Other parts of oropharynx","text":"Phenotype: Benign neoplasm: Other parts of oropharynx<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.623<br>N cases: 225<br>N controls: 377052"}
{"pvalue":0.0579,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm of other and ill-defined parts of digestive system","text":"Phenotype: Benign neoplasm of other and ill-defined parts of digestive system<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0579<br>N cases: 5062<br>N controls: 372215"}
{"pvalue":0.464,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of other and unspecified sites","text":"Phenotype: Benign neoplasm of other and unspecified sites<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.464<br>N cases: 866<br>N controls: 376411"}
{"pvalue":0.888,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm of ovary","text":"Phenotype: Benign neoplasm of ovary<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.888<br>N cases: 5308<br>N controls: 205562"}
{"pvalue":0.456,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Pancreas","text":"Phenotype: Benign neoplasm: Pancreas<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.456<br>N cases: 549<br>N controls: 376728"}
{"pvalue":0.0391,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Parathyroid gland","text":"Phenotype: Benign neoplasm: Parathyroid gland<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0391<br>N cases: 274<br>N controls: 377003"}
{"pvalue":0.535,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Parotid gland","text":"Phenotype: Benign neoplasm: Parotid gland<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.535<br>N cases: 2144<br>N controls: 375133"}
{"pvalue":0.375,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Pelvic bones, sacrum and coccyx","text":"Phenotype: Benign neoplasm: Pelvic bones, sacrum and coccyx<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.375<br>N cases: 80<br>N controls: 377197"}
{"pvalue":0.84,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Peripheral nerves and autonomic nervous system","text":"Phenotype: Benign neoplasm: Peripheral nerves and autonomic nervous system<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.84<br>N cases: 386<br>N controls: 376891"}
{"pvalue":0.991,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Pharynx, unspecified","text":"Phenotype: Benign neoplasm: Pharynx, unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.991<br>N cases: 182<br>N controls: 377095"}
{"pvalue":0.213,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Pituitary gland, craniopharyngeal duct","text":"Phenotype: Benign neoplasm: Pituitary gland, craniopharyngeal duct<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.213<br>N cases: 1402<br>N controls: 375875"}
{"pvalue":0.231,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Prostate","text":"Phenotype: Benign neoplasm: Prostate<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.231<br>N cases: 171<br>N controls: 166236"}
{"pvalue":0.403,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Rectosigmoid junction","text":"Phenotype: Benign neoplasm: Rectosigmoid junction<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.403<br>N cases: 982<br>N controls: 376295"}
{"pvalue":0.763,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Rectum/anal canal icd-9","text":"Phenotype: Benign neoplasm: Rectum/anal canal icd-9<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.763<br>N cases: 290<br>N controls: 376987"}
{"pvalue":0.647,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Rectum, anus and anal canal","text":"Phenotype: Benign neoplasm: Rectum, anus and anal canal<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.647<br>N cases: 5613<br>N controls: 371664"}
{"pvalue":0.704,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Rectum","text":"Phenotype: Benign neoplasm: Rectum<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.704<br>N cases: 4776<br>N controls: 372501"}
{"pvalue":0.885,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Retina","text":"Phenotype: Benign neoplasm: Retina<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.885<br>N cases: 125<br>N controls: 377152"}
{"pvalue":0.697,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of soft tissue of retroperitoneum and peritoneum","text":"Phenotype: Benign neoplasm of soft tissue of retroperitoneum and peritoneum<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.697<br>N cases: 138<br>N controls: 377139"}
{"pvalue":0.375,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of major salivary glands","text":"Phenotype: Benign neoplasm of major salivary glands<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.375<br>N cases: 2785<br>N controls: 374492"}
{"pvalue":0.253,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: salivary glands, exclude unknown (D119)","text":"Phenotype: Benign neoplasm: salivary glands, exclude unknown (D119)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.253<br>N cases: 2415<br>N controls: 374862"}
{"pvalue":0.492,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: other/unspecified salivary gland","text":"Phenotype: Benign neoplasm: other/unspecified salivary gland<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.492<br>N cases: 756<br>N controls: 376521"}
{"pvalue":0.349,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Scrotum","text":"Phenotype: Benign neoplasm: Scrotum<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.349<br>N cases: 99<br>N controls: 166308"}
{"pvalue":0.0461,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Sigmoid colon","text":"Phenotype: Benign neoplasm: Sigmoid colon<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0461<br>N cases: 4876<br>N controls: 372401"}
{"pvalue":0.572,"sign":-1,"group":"CD2: Neoplasms","label":"Other benign neoplasms of skin","text":"Phenotype: Other benign neoplasms of skin<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.572<br>N cases: 12341<br>N controls: 364936"}
{"pvalue":0.936,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Small intestine","text":"Phenotype: Benign neoplasm: Small intestine<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.936<br>N cases: 1031<br>N controls: 376246"}
{"pvalue":0.493,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Other and unspecified parts of small intestine","text":"Phenotype: Benign neoplasm: Other and unspecified parts of small intestine<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.493<br>N cases: 427<br>N controls: 376850"}
{"pvalue":0.501,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Spinal cord","text":"Phenotype: Benign neoplasm: Spinal cord<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.501<br>N cases: 355<br>N controls: 376922"}
{"pvalue":0.0179,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Stomach","text":"Phenotype: Benign neoplasm: Stomach<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0179<br>N cases: 2658<br>N controls: 374619"}
{"pvalue":0.0793,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Testis","text":"Phenotype: Benign neoplasm: Testis<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0793<br>N cases: 108<br>N controls: 166299"}
{"pvalue":0.769,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm of thyroid gland","text":"Phenotype: Benign neoplasm of thyroid gland<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.769<br>N cases: 875<br>N controls: 376402"}
{"pvalue":0.708,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Tongue","text":"Phenotype: Benign neoplasm: Tongue<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.708<br>N cases: 720<br>N controls: 376557"}
{"pvalue":0.205,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Tonsil","text":"Phenotype: Benign neoplasm: Tonsil<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.205<br>N cases: 281<br>N controls: 376996"}
{"pvalue":0.708,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Transverse colon","text":"Phenotype: Benign neoplasm: Transverse colon<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.708<br>N cases: 2404<br>N controls: 374873"}
{"pvalue":0.302,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm of urinary organs","text":"Phenotype: Benign neoplasm of urinary organs<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.302<br>N cases: 1165<br>N controls: 376112"}
{"pvalue":0.0537,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Uterine tubes and ligaments","text":"Phenotype: Benign neoplasm: Uterine tubes and ligaments<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0537<br>N cases: 163<br>N controls: 210707"}
{"pvalue":0.195,"sign":-1,"group":"CD2: Neoplasms","label":"Other benign neoplasm of uterus: Other parts/unspecified","text":"Phenotype: Other benign neoplasm of uterus: Other parts/unspecified<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.195<br>N cases: 1160<br>N controls: 209710"}
{"pvalue":0.236,"sign":-1,"group":"CD2: Neoplasms","label":"Other benign neoplasms of uterus","text":"Phenotype: Other benign neoplasms of uterus<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.236<br>N cases: 1477<br>N controls: 209393"}
{"pvalue":0.701,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Vulva","text":"Phenotype: Benign neoplasm: Vulva<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.701<br>N cases: 550<br>N controls: 210320"}
{"pvalue":0.423,"sign":-1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Vagina","text":"Phenotype: Benign neoplasm: Vagina<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.423<br>N cases: 325<br>N controls: 210545"}
{"pvalue":0.451,"sign":1,"group":"CD2: Neoplasms","label":"Benign neoplasm: Eye, unspecified (controls excluding all cancers)","text":"Phenotype: Benign neoplasm: Eye, unspecified (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.451<br>N cases: 113<br>N controls: 299881"}
{"pvalue":0.954,"sign":1,"group":"CD2: Neoplasms","label":"Follicular lymphoma (controls excluding all cancers)","text":"Phenotype: Follicular lymphoma (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.954<br>N cases: 1081<br>N controls: 299952"}
{"pvalue":0.962,"sign":1,"group":"CD2: Neoplasms","label":"Follicular lymphoma","text":"Phenotype: Follicular lymphoma<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.962<br>N cases: 1081<br>N controls: 376196"}
{"pvalue":0.23,"sign":1,"group":"CD2: Neoplasms","label":"Hodgkin lymphoma (controls excluding all cancers)","text":"Phenotype: Hodgkin lymphoma (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.23<br>N cases: 780<br>N controls: 299952"}
{"pvalue":0.25,"sign":1,"group":"CD2: Neoplasms","label":"Hodgkin lymphoma","text":"Phenotype: Hodgkin lymphoma<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.25<br>N cases: 780<br>N controls: 376497"}
{"pvalue":0.556,"sign":-1,"group":"CD2: Neoplasms","label":"Malignant immunoproliferative diseases (controls excluding all cancers)","text":"Phenotype: Malignant immunoproliferative diseases (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.556<br>N cases: 223<br>N controls: 299952"}
{"pvalue":0.0328,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ, bladder (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ, bladder (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0328<br>N cases: 654<br>N controls: 287130"}
{"pvalue":0.0723,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of breast (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of breast (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0723<br>N cases: 278<br>N controls: 167052"}
{"pvalue":0.882,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of breast, intraductal (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of breast, intraductal (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.882<br>N cases: 2219<br>N controls: 167070"}
{"pvalue":0.447,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of breast, lobular (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of breast, lobular (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.447<br>N cases: 167<br>N controls: 167176"}
{"pvalue":0.341,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of cervix uteri (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of cervix uteri (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.341<br>N cases: 2236<br>N controls: 165401"}
{"pvalue":0.477,"sign":-1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of colon (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of colon (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.477<br>N cases: 124<br>N controls: 287092"}
{"pvalue":0.528,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of endometrium (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of endometrium (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.528<br>N cases: 106<br>N controls: 167161"}
{"pvalue":0.583,"sign":-1,"group":"CD2: Neoplasms","label":"Melanoma in situ (controls excluding all cancers)","text":"Phenotype: Melanoma in situ (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.583<br>N cases: 887<br>N controls: 286876"}
{"pvalue":0.309,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of prostate (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of prostate (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.309<br>N cases: 141<br>N controls: 119882"}
{"pvalue":0.0641,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of rectum (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of rectum (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0641<br>N cases: 81<br>N controls: 287104"}
{"pvalue":0.516,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of skin (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of skin (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.516<br>N cases: 1911<br>N controls: 286158"}
{"pvalue":0.13,"sign":1,"group":"CD2: Neoplasms","label":"Carcinoma in situ of vulva (controls excluding all cancers)","text":"Phenotype: Carcinoma in situ of vulva (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.13<br>N cases: 155<br>N controls: 167097"}
{"pvalue":0.78,"sign":1,"group":"CD2: Neoplasms","label":"Leukaemia of unspecified cell type (controls excluding all cancers)","text":"Phenotype: Leukaemia of unspecified cell type (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.78<br>N cases: 220<br>N controls: 299952"}
{"pvalue":0.813,"sign":1,"group":"CD2: Neoplasms","label":"Leukaemia of unspecified cell type","text":"Phenotype: Leukaemia of unspecified cell type<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.813<br>N cases: 220<br>N controls: 377057"}
{"pvalue":0.583,"sign":1,"group":"CD2: Neoplasms","label":"Lymphoid leukaemia (controls excluding all cancers)","text":"Phenotype: Lymphoid leukaemia (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.583<br>N cases: 1493<br>N controls: 299952"}
{"pvalue":0.328,"sign":1,"group":"CD2: Neoplasms","label":"Multiple myeloma and malignant plasma cell neoplasms (controls excluding all cancers)","text":"Phenotype: Multiple myeloma and malignant plasma cell neoplasms (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.328<br>N cases: 1249<br>N controls: 299952"}
{"pvalue":0.209,"sign":1,"group":"CD2: Neoplasms","label":"Myeloid leukaemia (controls excluding all cancers)","text":"Phenotype: Myeloid leukaemia (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.209<br>N cases: 674<br>N controls: 299952"}
{"pvalue":0.221,"sign":1,"group":"CD2: Neoplasms","label":"Myeloid leukaemia","text":"Phenotype: Myeloid leukaemia<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.221<br>N cases: 674<br>N controls: 376603"}
{"pvalue":0.293,"sign":-1,"group":"CD2: Neoplasms","label":"Non-follicular lymphoma (controls excluding all cancers)","text":"Phenotype: Non-follicular lymphoma (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.293<br>N cases: 2602<br>N controls: 299952"}
{"pvalue":0.238,"sign":-1,"group":"CD2: Neoplasms","label":"Non-follicular lymphoma","text":"Phenotype: Non-follicular lymphoma<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.238<br>N cases: 2602<br>N controls: 374675"}
{"pvalue":0.73,"sign":-1,"group":"CD2: Neoplasms","label":"Other and unspecified types of non-Hodgkin lymphoma (controls excluding all cancers)","text":"Phenotype: Other and unspecified types of non-Hodgkin lymphoma (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.73<br>N cases: 1088<br>N controls: 299952"}
{"pvalue":0.765,"sign":-1,"group":"CD2: Neoplasms","label":"Other and unspecified types of non-Hodgkin lymphoma","text":"Phenotype: Other and unspecified types of non-Hodgkin lymphoma<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.765<br>N cases: 1088<br>N controls: 287137"}
{"pvalue":0.944,"sign":1,"group":"CD2: Neoplasms","label":"Primary_lymphoid and hematopoietic malignant neoplasms (controls excluding all cancers)","text":"Phenotype: Primary_lymphoid and hematopoietic malignant neoplasms (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.944<br>N cases: 7519<br>N controls: 299952"}
{"pvalue":0.977,"sign":-1,"group":"CD2: Neoplasms","label":"Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue (controls excluding all cancers)","text":"Phenotype: Other and unspecified malignant neoplasms of lymphoid, haematopoietic and related tissue (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.977<br>N cases: 248<br>N controls: 299952"}
{"pvalue":0.365,"sign":-1,"group":"CD2: Neoplasms","label":"Mature T/NK-cell lymphomas (controls excluding all cancers)","text":"Phenotype: Mature T/NK-cell lymphomas (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.365<br>N cases: 335<br>N controls: 299952"}
{"pvalue":0.526,"sign":1,"group":"CD2: Neoplasms","label":"Melanoma of uvea (controls excluding all cancers)","text":"Phenotype: Melanoma of uvea (controls excluding all cancers)<br>Category: CD2: Neoplasms<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.526<br>N cases: 242<br>N controls: 299884"}
{"pvalue":0.585,"sign":-1,"group":"AB1: Infectious diseases","label":"Enterocolitis due to Clostridium difficile","text":"Phenotype: Enterocolitis due to Clostridium difficile<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.585<br>N cases: 3118<br>N controls: 371656"}
{"pvalue":0.718,"sign":-1,"group":"AB1: Infectious diseases","label":"Other/unspecified cytomegaloviral diseases","text":"Phenotype: Other/unspecified cytomegaloviral diseases<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.718<br>N cases: 451<br>N controls: 376730"}
{"pvalue":0.505,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Acquired haemolytic anaemia","text":"Phenotype: Acquired haemolytic anaemia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.505<br>N cases: 606<br>N controls: 376439"}
{"pvalue":0.534,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified acquired haemolytic anaemias","text":"Phenotype: Other and unspecified acquired haemolytic anaemias<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.534<br>N cases: 241<br>N controls: 376439"}
{"pvalue":0.37,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Acquired pure red cell aplasia [erythroblastopenia]","text":"Phenotype: Acquired pure red cell aplasia [erythroblastopenia]<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.37<br>N cases: 126<br>N controls: 362319"}
{"pvalue":0.816,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Acute posthaemorrhagic anaemia","text":"Phenotype: Acute posthaemorrhagic anaemia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.816<br>N cases: 976<br>N controls: 362319"}
{"pvalue":0.171,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Agranulocytosis","text":"Phenotype: Agranulocytosis<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.171<br>N cases: 3234<br>N controls: 370400"}
{"pvalue":0.702,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other autoimmune haemolytic anaemias","text":"Phenotype: Other autoimmune haemolytic anaemias<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.702<br>N cases: 280<br>N controls: 376439"}
{"pvalue":0.163,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Allergic purpura","text":"Phenotype: Allergic purpura<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.163<br>N cases: 856<br>N controls: 371504"}
{"pvalue":0.152,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Vitamin B12 deficiency anaemia","text":"Phenotype: Vitamin B12 deficiency anaemia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.152<br>N cases: 3351<br>N controls: 360528"}
{"pvalue":0.0103,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Folate deficiency anaemia","text":"Phenotype: Folate deficiency anaemia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0103<br>N cases: 178<br>N controls: 360528"}
{"pvalue":0.274,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Anaemias","text":"Phenotype: Anaemias<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.274<br>N cases: 27371<br>N controls: 88536"}
{"pvalue":0.157,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Anaemia in chronic diseases classified elsewhere","text":"Phenotype: Anaemia in chronic diseases classified elsewhere<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.157<br>N cases: 585<br>N controls: 362319"}
{"pvalue":0.542,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Iron deficiency anaemia secondary to blood loss (chronic)","text":"Phenotype: Iron deficiency anaemia secondary to blood loss (chronic)<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.542<br>N cases: 4852<br>N controls: 360528"}
{"pvalue":0.987,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Iron deficiency anaemia","text":"Phenotype: Iron deficiency anaemia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.987<br>N cases: 13689<br>N controls: 360528"}
{"pvalue":0.714,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified iron deficiency","text":"Phenotype: Other and unspecified iron deficiency<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.714<br>N cases: 10208<br>N controls: 360528"}
{"pvalue":0.0641,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified anaemias","text":"Phenotype: Other and unspecified anaemias<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0641<br>N cases: 13600<br>N controls: 362319"}
{"pvalue":0.358,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified diseases of blood and blood-forming organs","text":"Phenotype: Other and unspecified diseases of blood and blood-forming organs<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.358<br>N cases: 633<br>N controls: 370400"}
{"pvalue":0.696,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other diseases of blood and blood-forming organs","text":"Phenotype: Other diseases of blood and blood-forming organs<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.696<br>N cases: 6877<br>N controls: 370400"}
{"pvalue":0.0423,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Chronic Coagulation defects","text":"Phenotype: Chronic Coagulation defects<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0423<br>N cases: 626<br>N controls: 376651"}
{"pvalue":0.0367,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified coagulation defects","text":"Phenotype: Other and unspecified coagulation defects<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0367<br>N cases: 1217<br>N controls: 371504"}
{"pvalue":0.475,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Coagulation defects, purpura and other haemorrhagic conditions","text":"Phenotype: Coagulation defects, purpura and other haemorrhagic conditions<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.475<br>N cases: 5773<br>N controls: 371504"}
{"pvalue":0.606,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other coagulation defects","text":"Phenotype: Other coagulation defects<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.606<br>N cases: 1904<br>N controls: 371504"}
{"pvalue":0.894,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Combined immunodeficiencies","text":"Phenotype: Combined immunodeficiencies<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.894<br>N cases: 305<br>N controls: 371255"}
{"pvalue":0.7,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Defects in the complement system","text":"Phenotype: Defects in the complement system<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.7<br>N cases: 171<br>N controls: 371255"}
{"pvalue":0.679,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Common variable immunodeficiency","text":"Phenotype: Common variable immunodeficiency<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.679<br>N cases: 171<br>N controls: 371255"}
{"pvalue":0.549,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other or unspecified common variable immunodeficiency","text":"Phenotype: Other or unspecified common variable immunodeficiency<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.549<br>N cases: 90<br>N controls: 371255"}
{"pvalue":0.863,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Selective deficiency of immunoglobulin G [IgG] subclasses","text":"Phenotype: Selective deficiency of immunoglobulin G [IgG] subclasses<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.863<br>N cases: 183<br>N controls: 371255"}
{"pvalue":0.853,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Selective deficiency of immunoglobulin A [IgA]y","text":"Phenotype: Selective deficiency of immunoglobulin A [IgA]y<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.853<br>N cases: 112<br>N controls: 371255"}
{"pvalue":0.484,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Disseminated intravascular coagulation [defibrination syndrome]","text":"Phenotype: Disseminated intravascular coagulation [defibrination syndrome]<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.484<br>N cases: 83<br>N controls: 371504"}
{"pvalue":0.42,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Familial erythrocytosis","text":"Phenotype: Familial erythrocytosis<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.42<br>N cases: 141<br>N controls: 370400"}
{"pvalue":0.21,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Haemolytic anaemias","text":"Phenotype: Haemolytic anaemias<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.21<br>N cases: 838<br>N controls: 376439"}
{"pvalue":0.0265,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Haemorrhagic disorder due to circulating anticoagulants","text":"Phenotype: Haemorrhagic disorder due to circulating anticoagulants<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0265<br>N cases: 267<br>N controls: 371504"}
{"pvalue":0.82,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified haemorrhagic conditions","text":"Phenotype: Other and unspecified haemorrhagic conditions<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.82<br>N cases: 404<br>N controls: 371504"}
{"pvalue":0.917,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other hereditary haemolytic anaemias","text":"Phenotype: Other hereditary haemolytic anaemias<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.917<br>N cases: 140<br>N controls: 376439"}
{"pvalue":0.564,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Hereditary hypogammaglobulinemia","text":"Phenotype: Hereditary hypogammaglobulinemia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.564<br>N cases: 99<br>N controls: 371255"}
{"pvalue":0.156,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Hereditary deficiency of other clotting factors","text":"Phenotype: Hereditary deficiency of other clotting factors<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.156<br>N cases: 216<br>N controls: 371504"}
{"pvalue":0.163,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Hypersplenism","text":"Phenotype: Hypersplenism<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.163<br>N cases: 105<br>N controls: 370400"}
{"pvalue":0.245,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Immunodeficiency with predominantly antibody defects","text":"Phenotype: Immunodeficiency with predominantly antibody defects<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.245<br>N cases: 711<br>N controls: 371255"}
{"pvalue":0.0815,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified immunodeficiencies with predominantly antibody defects","text":"Phenotype: Other and unspecified immunodeficiencies with predominantly antibody defects<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0815<br>N cases: 336<br>N controls: 371255"}
{"pvalue":0.706,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Immunodeficiencies","text":"Phenotype: Immunodeficiencies<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.706<br>N cases: 1350<br>N controls: 375927"}
{"pvalue":0.721,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other or unspecified immunodeficiency","text":"Phenotype: Other or unspecified immunodeficiency<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.721<br>N cases: 97<br>N controls: 371255"}
{"pvalue":0.609,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other immunodeficiencies","text":"Phenotype: Other immunodeficiencies<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.609<br>N cases: 285<br>N controls: 371255"}
{"pvalue":0.982,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Certain disorders involving the immune mechanism","text":"Phenotype: Certain disorders involving the immune mechanism<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.982<br>N cases: 6022<br>N controls: 371255"}
{"pvalue":0.516,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Infarction of spleen","text":"Phenotype: Infarction of spleen<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.516<br>N cases: 123<br>N controls: 370400"}
{"pvalue":0.352,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Idiopathic thrombocytopenic purpura","text":"Phenotype: Idiopathic thrombocytopenic purpura<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.352<br>N cases: 810<br>N controls: 371504"}
{"pvalue":0.726,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Kela reimbursement Agammaglobulinemia (D80-84)","text":"Phenotype: Kela reimbursement Agammaglobulinemia (D80-84)<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.726<br>N cases: 202<br>N controls: 371255"}
{"pvalue":0.648,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Nezelof syndrome","text":"Phenotype: Nezelof syndrome<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.648<br>N cases: 125<br>N controls: 371255"}
{"pvalue":0.302,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Nonhereditary hypogammaglobulinemia","text":"Phenotype: Nonhereditary hypogammaglobulinemia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.302<br>N cases: 279<br>N controls: 371255"}
{"pvalue":0.696,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other nutritional anaemias","text":"Phenotype: Other nutritional anaemias<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.696<br>N cases: 283<br>N controls: 360528"}
{"pvalue":0.552,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue","text":"Phenotype: Other specified diseases with participation of lymphoreticular and reticulohistiocytic tissue<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.552<br>N cases: 86<br>N controls: 370400"}
{"pvalue":0.561,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified aplastic anaemias","text":"Phenotype: Other and unspecified aplastic anaemias<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.561<br>N cases: 288<br>N controls: 362319"}
{"pvalue":0.346,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other diseases of blood and blood-forming organs","text":"Phenotype: Other diseases of blood and blood-forming organs<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.346<br>N cases: 1892<br>N controls: 370400"}
{"pvalue":0.612,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other disorders of white blood cells","text":"Phenotype: Other disorders of white blood cells<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.612<br>N cases: 1483<br>N controls: 370400"}
{"pvalue":0.74,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other nonthrombocytopenic purpura","text":"Phenotype: Other nonthrombocytopenic purpura<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.74<br>N cases: 214<br>N controls: 371504"}
{"pvalue":0.785,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other primary thrombocytopenia","text":"Phenotype: Other primary thrombocytopenia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.785<br>N cases: 88<br>N controls: 371504"}
{"pvalue":0.561,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Purpura and other haemorrhagic conditions","text":"Phenotype: Purpura and other haemorrhagic conditions<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.561<br>N cases: 3900<br>N controls: 371504"}
{"pvalue":0.824,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Qualitative platelet defects","text":"Phenotype: Qualitative platelet defects<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.824<br>N cases: 112<br>N controls: 371504"}
{"pvalue":0.321,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Sarcoidosis","text":"Phenotype: Sarcoidosis<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.321<br>N cases: 4041<br>N controls: 371255"}
{"pvalue":0.39,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Severe combined immunodeficiency [SCID] with reticular dysgenesis","text":"Phenotype: Severe combined immunodeficiency [SCID] with reticular dysgenesis<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.39<br>N cases: 82<br>N controls: 371255"}
{"pvalue":0.574,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Secondary polycythaemia","text":"Phenotype: Secondary polycythaemia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.574<br>N cases: 608<br>N controls: 370400"}
{"pvalue":0.834,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Secondary thrombocytopenia","text":"Phenotype: Secondary thrombocytopenia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.834<br>N cases: 298<br>N controls: 371504"}
{"pvalue":0.561,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Hereditary sideroblastic anaemia","text":"Phenotype: Hereditary sideroblastic anaemia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.561<br>N cases: 103<br>N controls: 362319"}
{"pvalue":0.403,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Other sideroblastic anaemias","text":"Phenotype: Other sideroblastic anaemias<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.403<br>N cases: 102<br>N controls: 362319"}
{"pvalue":0.0572,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Diseases of spleen","text":"Phenotype: Diseases of spleen<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0572<br>N cases: 397<br>N controls: 370400"}
{"pvalue":0.106,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified diseases of spleen","text":"Phenotype: Other and unspecified diseases of spleen<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.106<br>N cases: 92<br>N controls: 370400"}
{"pvalue":0.801,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Thrombocytopenia, unspecified","text":"Phenotype: Thrombocytopenia, unspecified<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.801<br>N cases: 1869<br>N controls: 371504"}
{"pvalue":0.0274,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Von Willebrand disease","text":"Phenotype: Von Willebrand disease<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0274<br>N cases: 336<br>N controls: 371504"}
{"pvalue":0.877,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Other and unspecified disorders of white blood cells","text":"Phenotype: Other and unspecified disorders of white blood cells<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.877<br>N cases: 1077<br>N controls: 370400"}
{"pvalue":0.601,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Drug-induced adrenocortical insufficiency","text":"Phenotype: Drug-induced adrenocortical insufficiency<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.601<br>N cases: 403<br>N controls: 376874"}
{"pvalue":0.348,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Drug-induced cataract","text":"Phenotype: Drug-induced cataract<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.348<br>N cases: 621<br>N controls: 376656"}
{"pvalue":0.232,"sign":1,"group":"G6: Nervous system diseases","label":"Drug-induced dystonia","text":"Phenotype: Drug-induced dystonia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.232<br>N cases: 86<br>N controls: 377191"}
{"pvalue":0.851,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Drug-induced gout","text":"Phenotype: Drug-induced gout<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.851<br>N cases: 121<br>N controls: 377156"}
{"pvalue":0.889,"sign":1,"group":"G6: Nervous system diseases","label":"Drug-induced headache, not elsewhere classified","text":"Phenotype: Drug-induced headache, not elsewhere classified<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.889<br>N cases: 132<br>N controls: 377145"}
{"pvalue":0.21,"sign":-1,"group":"D3: Blood and blood-forming organ diseases","label":"Drug-induced neutropenia","text":"Phenotype: Drug-induced neutropenia<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.21<br>N cases: 1978<br>N controls: 375299"}
{"pvalue":0.99,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Drug-induced osteoporosis","text":"Phenotype: Drug-induced osteoporosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.99<br>N cases: 289<br>N controls: 376988"}
{"pvalue":0.647,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Drug-induced systemic lupus erythematosus","text":"Phenotype: Drug-induced systemic lupus erythematosus<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.647<br>N cases: 191<br>N controls: 377086"}
{"pvalue":0.368,"sign":-1,"group":"G6: Nervous system diseases","label":"Drug-induced tremor","text":"Phenotype: Drug-induced tremor<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.368<br>N cases: 151<br>N controls: 377126"}
{"pvalue":0.948,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Dry age-related macular degeneration (includes geographic atrophy)","text":"Phenotype: Dry age-related macular degeneration (includes geographic atrophy)<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.948<br>N cases: 6065<br>N controls: 251042"}
{"pvalue":0.409,"sign":-1,"group":"K11: Digestive system diseases","label":"Duodenal ulcer - Unspecified as acute or chronic, without haemorrhage or perforation, drug-induced","text":"Phenotype: Duodenal ulcer - Unspecified as acute or chronic, without haemorrhage or perforation, drug-induced<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.409<br>N cases: 106<br>N controls: 377171"}
{"pvalue":0.678,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Acidosis","text":"Phenotype: Acidosis<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.678<br>N cases: 479<br>N controls: 324150"}
{"pvalue":0.639,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Acromegaly and pituitary gigantism","text":"Phenotype: Acromegaly and pituitary gigantism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.639<br>N cases: 183<br>N controls: 361988"}
{"pvalue":0.85,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Adrenocortical insufficiency","text":"Phenotype: Adrenocortical insufficiency<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.85<br>N cases: 923<br>N controls: 361988"}
{"pvalue":0.405,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Other adrenocortical overactivity","text":"Phenotype: Other adrenocortical overactivity<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.405<br>N cases: 146<br>N controls: 361988"}
{"pvalue":0.424,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Adrenomedullary hyperfunction","text":"Phenotype: Adrenomedullary hyperfunction<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.424<br>N cases: 80<br>N controls: 361988"}
{"pvalue":0.336,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of adrenal gland, other and/or unspecified","text":"Phenotype: Disorders of adrenal gland, other and/or unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.336<br>N cases: 129<br>N controls: 361988"}
{"pvalue":0.29,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Adrenogenital disorders","text":"Phenotype: Adrenogenital disorders<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.29<br>N cases: 127<br>N controls: 361988"}
{"pvalue":0.0817,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Other disorders of amino-acid metabolism","text":"Phenotype: Other disorders of amino-acid metabolism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0817<br>N cases: 127<br>N controls: 324150"}
{"pvalue":0.151,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Amyloidosis, other/unspecified","text":"Phenotype: Amyloidosis, other/unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.151<br>N cases: 413<br>N controls: 324150"}
{"pvalue":0.388,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Secondary systemic amyloidosis","text":"Phenotype: Secondary systemic amyloidosis<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.388<br>N cases: 88<br>N controls: 324150"}
{"pvalue":0.743,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Syndrome of inappropriate secretion of antidiuretic hormone","text":"Phenotype: Syndrome of inappropriate secretion of antidiuretic hormone<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.743<br>N cases: 119<br>N controls: 361988"}
{"pvalue":0.406,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of aromatic amino-acid metabolism","text":"Phenotype: Disorders of aromatic amino-acid metabolism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.406<br>N cases: 93<br>N controls: 324150"}
{"pvalue":0.206,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Other disorders of carbohydrate metabolism","text":"Phenotype: Other disorders of carbohydrate metabolism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.206<br>N cases: 127<br>N controls: 324150"}
{"pvalue":0.922,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorder of carbohydrate metabolism, other/unspecified","text":"Phenotype: Disorder of carbohydrate metabolism, other/unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.922<br>N cases: 84<br>N controls: 324150"}
{"pvalue":0.0114,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Carcinoid syndrome","text":"Phenotype: Carcinoid syndrome<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0114<br>N cases: 249<br>N controls: 361988"}
{"pvalue":0.885,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Congenital iodine-deficiency syndrome/hypothyroidism","text":"Phenotype: Congenital iodine-deficiency syndrome/hypothyroidism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.885<br>N cases: 877<br>N controls: 320703"}
{"pvalue":0.679,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Cushing syndrome","text":"Phenotype: Cushing syndrome<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.679<br>N cases: 293<br>N controls: 361988"}
{"pvalue":0.503,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Delayed puberty","text":"Phenotype: Delayed puberty<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.503<br>N cases: 213<br>N controls: 361988"}
{"pvalue":0.983,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Diabetes insipidus","text":"Phenotype: Diabetes insipidus<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.983<br>N cases: 245<br>N controls: 361988"}
{"pvalue":0.374,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of puberty","text":"Phenotype: Disorders of puberty<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.374<br>N cases: 412<br>N controls: 361988"}
{"pvalue":0.127,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 1 diabetes with coma","text":"Phenotype: Type 1 diabetes with coma<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.127<br>N cases: 2050<br>N controls: 308280"}
{"pvalue":0.274,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 1 diabetes with ketoacidosis","text":"Phenotype: Type 1 diabetes with ketoacidosis<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.274<br>N cases: 2102<br>N controls: 308280"}
{"pvalue":0.264,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 1 diabetes with other specified/multiple/unspecified complications","text":"Phenotype: Type 1 diabetes with other specified/multiple/unspecified complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.264<br>N cases: 6234<br>N controls: 308280"}
{"pvalue":0.359,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 1 diabetes with neurological complications","text":"Phenotype: Type 1 diabetes with neurological complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.359<br>N cases: 1077<br>N controls: 308280"}
{"pvalue":0.0875,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 1 diabetes with ophthalmic complications","text":"Phenotype: Type 1 diabetes with ophthalmic complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0875<br>N cases: 5202<br>N controls: 308280"}
{"pvalue":0.808,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 1 diabetes with peripheral circulatory complications","text":"Phenotype: Type 1 diabetes with peripheral circulatory complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.808<br>N cases: 669<br>N controls: 308280"}
{"pvalue":0.556,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 1 diabetes with renal complications","text":"Phenotype: Type 1 diabetes with renal complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.556<br>N cases: 1579<br>N controls: 308280"}
{"pvalue":0.718,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 2 diabetes with coma","text":"Phenotype: Type 2 diabetes with coma<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.718<br>N cases: 4709<br>N controls: 308280"}
{"pvalue":0.873,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 2 diabetes with ketoacidosis","text":"Phenotype: Type 2 diabetes with ketoacidosis<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.873<br>N cases: 657<br>N controls: 308280"}
{"pvalue":0.00625,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 2 diabetes with other specified/multiple/unspecified complications","text":"Phenotype: Type 2 diabetes with other specified/multiple/unspecified complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00625<br>N cases: 46373<br>N controls: 308280"}
{"pvalue":0.631,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 2 diabetes with neurological complications","text":"Phenotype: Type 2 diabetes with neurological complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.631<br>N cases: 1894<br>N controls: 308280"}
{"pvalue":0.0314,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 2 diabetes with ophthalmic complications","text":"Phenotype: Type 2 diabetes with ophthalmic complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0314<br>N cases: 4172<br>N controls: 308280"}
{"pvalue":0.136,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 2 diabetes with peripheral circulatory complications","text":"Phenotype: Type 2 diabetes with peripheral circulatory complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.136<br>N cases: 2179<br>N controls: 308280"}
{"pvalue":0.601,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Type 2 diabetes with renal complications","text":"Phenotype: Type 2 diabetes with renal complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.601<br>N cases: 2684<br>N controls: 308280"}
{"pvalue":0.536,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Unspecified diabetes with coma","text":"Phenotype: Unspecified diabetes with coma<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.536<br>N cases: 158<br>N controls: 308280"}
{"pvalue":0.214,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Unspecified diabetes","text":"Phenotype: Unspecified diabetes<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.214<br>N cases: 7455<br>N controls: 308280"}
{"pvalue":0.816,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Unspecified diabetes with ketoacidosis","text":"Phenotype: Unspecified diabetes with ketoacidosis<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.816<br>N cases: 259<br>N controls: 308280"}
{"pvalue":0.928,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Unspecified diabetes with multiple/unspecified complications","text":"Phenotype: Unspecified diabetes with multiple/unspecified complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.928<br>N cases: 1039<br>N controls: 308280"}
{"pvalue":0.981,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Unspecified diabetes with neurological complications","text":"Phenotype: Unspecified diabetes with neurological complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.981<br>N cases: 104<br>N controls: 308280"}
{"pvalue":0.35,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Unspecified diabetes without complications","text":"Phenotype: Unspecified diabetes without complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.35<br>N cases: 2855<br>N controls: 308280"}
{"pvalue":0.329,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Unspecified diabetes with ophthalmic complications","text":"Phenotype: Unspecified diabetes with ophthalmic complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.329<br>N cases: 88<br>N controls: 308280"}
{"pvalue":0.981,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Unspecified diabetes with other specified complications","text":"Phenotype: Unspecified diabetes with other specified complications<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.981<br>N cases: 138<br>N controls: 308280"}
{"pvalue":0.881,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Other endocrine disorders","text":"Phenotype: Other endocrine disorders<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.881<br>N cases: 1576<br>N controls: 361988"}
{"pvalue":0.124,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Endocrine disorders, other/unspecified","text":"Phenotype: Endocrine disorders, other/unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.124<br>N cases: 588<br>N controls: 361988"}
{"pvalue":0.679,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of other endocrine glands","text":"Phenotype: Disorders of other endocrine glands<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.679<br>N cases: 15289<br>N controls: 361988"}
{"pvalue":0.908,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Postprocedural endocrine and metabolic disorders, not elsewhere classified","text":"Phenotype: Postprocedural endocrine and metabolic disorders, not elsewhere classified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.908<br>N cases: 3383<br>N controls: 324150"}
{"pvalue":0.665,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Iron deficiency","text":"Phenotype: Iron deficiency<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.665<br>N cases: 340<br>N controls: 354812"}
{"pvalue":0.463,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Familial hypercholesterolemia","text":"Phenotype: Familial hypercholesterolemia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.463<br>N cases: 4965<br>N controls: 324150"}
{"pvalue":0.222,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Familial hypercholesterolemia, with ischemic heart disease","text":"Phenotype: Familial hypercholesterolemia, with ischemic heart disease<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.222<br>N cases: 2757<br>N controls: 313533"}
{"pvalue":0.97,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Other disorders of fluid, electrolyte and acid-base balance","text":"Phenotype: Other disorders of fluid, electrolyte and acid-base balance<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.97<br>N cases: 9694<br>N controls: 324150"}
{"pvalue":0.158,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Other disorders of electrolyte and fluid balance, not elsewhere classified","text":"Phenotype: Other disorders of electrolyte and fluid balance, not elsewhere classified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.158<br>N cases: 226<br>N controls: 324150"}
{"pvalue":0.431,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Gilbert syndrome","text":"Phenotype: Gilbert syndrome<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.431<br>N cases: 180<br>N controls: 324150"}
{"pvalue":0.231,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Other disorders of glucose regulation and pancreatic internal secretion","text":"Phenotype: Other disorders of glucose regulation and pancreatic internal secretion<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.231<br>N cases: 2583<br>N controls: 374694"}
{"pvalue":0.634,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Nontoxic diffuse goitre","text":"Phenotype: Nontoxic diffuse goitre<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.634<br>N cases: 838<br>N controls: 320703"}
{"pvalue":0.19,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Nontoxic multinodular goitre","text":"Phenotype: Nontoxic multinodular goitre<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.19<br>N cases: 6149<br>N controls: 320703"}
{"pvalue":0.413,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Other and/or unspecified nontoxic goitre","text":"Phenotype: Other and/or unspecified nontoxic goitre<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.413<br>N cases: 2334<br>N controls: 320703"}
{"pvalue":0.722,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Nontoxic single thyroid nodule","text":"Phenotype: Nontoxic single thyroid nodule<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.722<br>N cases: 2027<br>N controls: 320703"}
{"pvalue":0.565,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Graves ophthalmopathy, strict","text":"Phenotype: Graves ophthalmopathy, strict<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.565<br>N cases: 561<br>N controls: 376716"}
{"pvalue":0.882,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Graves disease, strict definition","text":"Phenotype: Graves disease, strict definition<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.882<br>N cases: 2836<br>N controls: 374441"}
{"pvalue":0.337,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hyperaldosteronism","text":"Phenotype: Hyperaldosteronism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.337<br>N cases: 690<br>N controls: 361988"}
{"pvalue":0.0271,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Pure hypercholesterolaemia","text":"Phenotype: Pure hypercholesterolaemia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0271<br>N cases: 25928<br>N controls: 324150"}
{"pvalue":0.681,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Pure hyperglyceridaemia","text":"Phenotype: Pure hyperglyceridaemia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.681<br>N cases: 565<br>N controls: 324150"}
{"pvalue":0.788,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hyperkalaemia","text":"Phenotype: Hyperkalaemia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.788<br>N cases: 1455<br>N controls: 324150"}
{"pvalue":0.261,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Mixed hyperlipidaemia","text":"Phenotype: Mixed hyperlipidaemia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.261<br>N cases: 1084<br>N controls: 324150"}
{"pvalue":0.786,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hyperlipidaemia, other/unspecified","text":"Phenotype: Hyperlipidaemia, other/unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.786<br>N cases: 12304<br>N controls: 324150"}
{"pvalue":0.0503,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hyperosmolality and hypernatraemia","text":"Phenotype: Hyperosmolality and hypernatraemia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0503<br>N cases: 328<br>N controls: 324150"}
{"pvalue":0.0617,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hyperparathyroidism","text":"Phenotype: Hyperparathyroidism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0617<br>N cases: 5590<br>N controls: 361988"}
{"pvalue":0.439,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hyperfunction of pituitary gland","text":"Phenotype: Hyperfunction of pituitary gland<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.439<br>N cases: 1460<br>N controls: 361988"}
{"pvalue":0.836,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hyperprolactinaemia, drug-induced","text":"Phenotype: Hyperprolactinaemia, drug-induced<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.836<br>N cases: 160<br>N controls: 377117"}
{"pvalue":0.386,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hyperprolactinaemia","text":"Phenotype: Hyperprolactinaemia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.386<br>N cases: 1014<br>N controls: 361988"}
{"pvalue":0.18,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease","text":"Phenotype: Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.18<br>N cases: 116<br>N controls: 324150"}
{"pvalue":0.753,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Nondiabetic hypoglycaemic coma","text":"Phenotype: Nondiabetic hypoglycaemic coma<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.753<br>N cases: 122<br>N controls: 374694"}
{"pvalue":0.00846,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Drug-induced hypoglycaemia without coma","text":"Phenotype: Drug-induced hypoglycaemia without coma<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00846<br>N cases: 445<br>N controls: 374694"}
{"pvalue":0.149,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hypokalaemia","text":"Phenotype: Hypokalaemia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.149<br>N cases: 3278<br>N controls: 324150"}
{"pvalue":0.407,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hypo-osmolality and hyponatraemia","text":"Phenotype: Hypo-osmolality and hyponatraemia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.407<br>N cases: 5137<br>N controls: 324150"}
{"pvalue":0.451,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hypoparathyroidism","text":"Phenotype: Hypoparathyroidism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.451<br>N cases: 899<br>N controls: 361988"}
{"pvalue":0.139,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hypopituitarism","text":"Phenotype: Hypopituitarism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.139<br>N cases: 1902<br>N controls: 361988"}
{"pvalue":0.955,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hypothyroidism, autoimmune, DX-based","text":"Phenotype: Hypothyroidism, autoimmune, DX-based<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.955<br>N cases: 92<br>N controls: 376788"}
{"pvalue":0.166,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hypothyroidism, strict autoimmune","text":"Phenotype: Hypothyroidism, strict autoimmune<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.166<br>N cases: 40926<br>N controls: 274069"}
{"pvalue":0.33,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Postinfectious hypothyroidism","text":"Phenotype: Postinfectious hypothyroidism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.33<br>N cases: 158<br>N controls: 320703"}
{"pvalue":0.611,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hypothyroidism due to medicaments and other exogenous substances","text":"Phenotype: Hypothyroidism due to medicaments and other exogenous substances<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.611<br>N cases: 258<br>N controls: 320703"}
{"pvalue":0.434,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of iron metabolism","text":"Phenotype: Disorders of iron metabolism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.434<br>N cases: 324<br>N controls: 324150"}
{"pvalue":0.37,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Lactose intolerance, other/unspecified","text":"Phenotype: Lactose intolerance, other/unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.37<br>N cases: 691<br>N controls: 324150"}
{"pvalue":0.0253,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of lipoprotein metabolism and other lipidaemias","text":"Phenotype: Disorders of lipoprotein metabolism and other lipidaemias<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0253<br>N cases: 37742<br>N controls: 324150"}
{"pvalue":0.803,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorder of lipoprotein metabolism, unspecified","text":"Phenotype: Disorder of lipoprotein metabolism, unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.803<br>N cases: 3989<br>N controls: 324150"}
{"pvalue":0.534,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Localized adiposity","text":"Phenotype: Localized adiposity<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.534<br>N cases: 132<br>N controls: 355786"}
{"pvalue":0.949,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Malnutrition","text":"Phenotype: Malnutrition<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.949<br>N cases: 469<br>N controls: 376808"}
{"pvalue":0.0391,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Metabolic disorders","text":"Phenotype: Metabolic disorders<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0391<br>N cases: 53127<br>N controls: 324150"}
{"pvalue":0.313,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of magnesium metabolism","text":"Phenotype: Disorders of magnesium metabolism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.313<br>N cases: 154<br>N controls: 324150"}
{"pvalue":0.615,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of mineral metabolism","text":"Phenotype: Disorders of mineral metabolism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.615<br>N cases: 2215<br>N controls: 324150"}
{"pvalue":0.111,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Nontoxic goitre/thyroid nodule","text":"Phenotype: Nontoxic goitre/thyroid nodule<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.111<br>N cases: 9485<br>N controls: 367792"}
{"pvalue":0.476,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Other specified/unspecified nutritional deficiencies","text":"Phenotype: Other specified/unspecified nutritional deficiencies<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.476<br>N cases: 205<br>N controls: 354812"}
{"pvalue":0.85,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Obesity due to excess calories","text":"Phenotype: Obesity due to excess calories<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.85<br>N cases: 15045<br>N controls: 355902"}
{"pvalue":0.145,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Drug-induced obesity","text":"Phenotype: Drug-induced obesity<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.145<br>N cases: 240<br>N controls: 355902"}
{"pvalue":0.56,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Obesity","text":"Phenotype: Obesity<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.56<br>N cases: 21375<br>N controls: 355786"}
{"pvalue":0.355,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Obesity, other/unspecified","text":"Phenotype: Obesity, other/unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.355<br>N cases: 11025<br>N controls: 355902"}
{"pvalue":0.477,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Extreme obesity with alveolar hypoventilation","text":"Phenotype: Extreme obesity with alveolar hypoventilation<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.477<br>N cases: 1064<br>N controls: 355902"}
{"pvalue":0.0724,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Ovarian dysfunction","text":"Phenotype: Ovarian dysfunction<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0724<br>N cases: 2010<br>N controls: 200581"}
{"pvalue":0.447,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Ovarian dysfunction, other/unspecified","text":"Phenotype: Ovarian dysfunction, other/unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.447<br>N cases: 127<br>N controls: 200581"}
{"pvalue":0.51,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Primary ovarian failure","text":"Phenotype: Primary ovarian failure<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.51<br>N cases: 469<br>N controls: 200581"}
{"pvalue":0.27,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorder of pancreatic internal secretion, other and/or unspecified","text":"Phenotype: Disorder of pancreatic internal secretion, other and/or unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.27<br>N cases: 188<br>N controls: 374694"}
{"pvalue":0.489,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of parathyroid gland, other and/or unspecified","text":"Phenotype: Disorders of parathyroid gland, other and/or unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.489<br>N cases: 193<br>N controls: 361988"}
{"pvalue":0.203,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of parathyroid gland","text":"Phenotype: Disorders of parathyroid gland<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.203<br>N cases: 6362<br>N controls: 361988"}
{"pvalue":0.0378,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Polycystic ovarian syndrome, broad definition","text":"Phenotype: Polycystic ovarian syndrome, broad definition<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0378<br>N cases: 3205<br>N controls: 204492"}
{"pvalue":0.0488,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Polycystic ovarian syndrome, consortium definition","text":"Phenotype: Polycystic ovarian syndrome, consortium definition<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0488<br>N cases: 31548<br>N controls: 179322"}
{"pvalue":0.0365,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Polycystic ovarian syndrome","text":"Phenotype: Polycystic ovarian syndrome<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0365<br>N cases: 1424<br>N controls: 200581"}
{"pvalue":0.0157,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of phosphorus metabolism and phosphatases","text":"Phenotype: Disorders of phosphorus metabolism and phosphatases<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0157<br>N cases: 109<br>N controls: 324150"}
{"pvalue":0.596,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of pituitary gland, other and/or unspecified","text":"Phenotype: Disorders of pituitary gland, other and/or unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.596<br>N cases: 148<br>N controls: 361988"}
{"pvalue":0.471,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of plasma-protein metabolism, not elsewhere classified","text":"Phenotype: Disorders of plasma-protein metabolism, not elsewhere classified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.471<br>N cases: 176<br>N controls: 324150"}
{"pvalue":0.0893,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of porphyrin and bilirubin metabolism","text":"Phenotype: Disorders of porphyrin and bilirubin metabolism<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0893<br>N cases: 284<br>N controls: 324150"}
{"pvalue":0.817,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Precocious central puberty","text":"Phenotype: Precocious central puberty<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.817<br>N cases: 171<br>N controls: 361988"}
{"pvalue":0.591,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Precocious puberty","text":"Phenotype: Precocious puberty<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.591<br>N cases: 123<br>N controls: 361988"}
{"pvalue":0.169,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Protein-energy malnutrition of moderate and mild degree","text":"Phenotype: Protein-energy malnutrition of moderate and mild degree<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.169<br>N cases: 193<br>N controls: 376808"}
{"pvalue":0.439,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Unspecified protein-energy malnutrition","text":"Phenotype: Unspecified protein-energy malnutrition<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.439<br>N cases: 116<br>N controls: 376808"}
{"pvalue":0.116,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of puberty, other/unspecified","text":"Phenotype: Disorders of puberty, other/unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.116<br>N cases: 105<br>N controls: 361988"}
{"pvalue":0.584,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Short stature, not elsewhere classified","text":"Phenotype: Short stature, not elsewhere classified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.584<br>N cases: 611<br>N controls: 361988"}
{"pvalue":0.476,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of sphingolipid metabolism and other lipid storage disorders","text":"Phenotype: Disorders of sphingolipid metabolism and other lipid storage disorders<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.476<br>N cases: 98<br>N controls: 324150"}
{"pvalue":0.11,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Constitutional tall stature","text":"Phenotype: Constitutional tall stature<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.11<br>N cases: 126<br>N controls: 361988"}
{"pvalue":0.3,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Testicular dysfunction, other/unspecified","text":"Phenotype: Testicular dysfunction, other/unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.3<br>N cases: 91<br>N controls: 161407"}
{"pvalue":0.129,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Testicular hypofunction","text":"Phenotype: Testicular hypofunction<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.129<br>N cases: 667<br>N controls: 161407"}
{"pvalue":0.554,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Thiamine deficiency","text":"Phenotype: Thiamine deficiency<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.554<br>N cases: 137<br>N controls: 354812"}
{"pvalue":0.582,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorders of the thyroid gland","text":"Phenotype: Disorders of the thyroid gland<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.582<br>N cases: 56574<br>N controls: 320703"}
{"pvalue":0.167,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Acute thyroiditis","text":"Phenotype: Acute thyroiditis<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.167<br>N cases: 109<br>N controls: 320703"}
{"pvalue":0.886,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Autoimmune thyroiditis","text":"Phenotype: Autoimmune thyroiditis<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.886<br>N cases: 489<br>N controls: 320703"}
{"pvalue":0.0646,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Chronic thyroiditis","text":"Phenotype: Chronic thyroiditis<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0646<br>N cases: 108<br>N controls: 320703"}
{"pvalue":0.0669,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Thyroiditis, unspecified","text":"Phenotype: Thyroiditis, unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0669<br>N cases: 403<br>N controls: 320703"}
{"pvalue":0.766,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Subacute thyroiditis","text":"Phenotype: Subacute thyroiditis<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.766<br>N cases: 742<br>N controls: 320703"}
{"pvalue":0.898,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Disorder of thyroid, unspecified","text":"Phenotype: Disorder of thyroid, unspecified<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.898<br>N cases: 286<br>N controls: 320703"}
{"pvalue":0.0482,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Thyrotoxicosis factitia","text":"Phenotype: Thyrotoxicosis factitia<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0482<br>N cases: 87<br>N controls: 369104"}
{"pvalue":0.624,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Thyrotoxicosis with diffuse goitre","text":"Phenotype: Thyrotoxicosis with diffuse goitre<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.624<br>N cases: 4462<br>N controls: 320703"}
{"pvalue":0.362,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Thyrotoxicosis with toxic multinodular goitre","text":"Phenotype: Thyrotoxicosis with toxic multinodular goitre<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.362<br>N cases: 1600<br>N controls: 369104"}
{"pvalue":0.437,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Thyrotoxicosis with toxic single thyroid nodule","text":"Phenotype: Thyrotoxicosis with toxic single thyroid nodule<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.437<br>N cases: 232<br>N controls: 369104"}
{"pvalue":0.245,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Vitamin A deficiency","text":"Phenotype: Vitamin A deficiency<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.245<br>N cases: 120<br>N controls: 354812"}
{"pvalue":0.525,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Deficiency of other B group vitamins","text":"Phenotype: Deficiency of other B group vitamins<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.525<br>N cases: 599<br>N controls: 354812"}
{"pvalue":0.00056,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Vitamin D deficiency","text":"Phenotype: Vitamin D deficiency<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.000562<br>N cases: 426<br>N controls: 354812"}
{"pvalue":0.0576,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Volume depletion","text":"Phenotype: Volume depletion<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0576<br>N cases: 2676<br>N controls: 324150"}
{"pvalue":0.0333,"sign":1,"group":"G6: Nervous system diseases","label":"Epileptic seizures related to drugs","text":"Phenotype: Epileptic seizures related to drugs<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0333<br>N cases: 91<br>N controls: 377186"}
{"pvalue":0.383,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Erectile dysfunction","text":"Phenotype: Erectile dysfunction<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.383<br>N cases: 2205<br>N controls: 164104"}
{"pvalue":0.0447,"sign":1,"group":"D3: Blood and blood-forming organ diseases","label":"Eosinophilic disease (BM)","text":"Phenotype: Eosinophilic disease (BM)<br>Category: D3: Blood and blood-forming organ diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0447<br>N cases: 398<br>N controls: 212144"}
{"pvalue":0.127,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Disturbance of activity and attention","text":"Phenotype: Disturbance of activity and attention<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.127<br>N cases: 2340<br>N controls: 371117"}
{"pvalue":0.736,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Agoraphobia","text":"Phenotype: Agoraphobia<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.736<br>N cases: 890<br>N controls: 337577"}
{"pvalue":0.842,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Acute alcohol intoxication","text":"Phenotype: Acute alcohol intoxication<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.842<br>N cases: 8957<br>N controls: 353355"}
{"pvalue":0.405,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Alcohol dependence","text":"Phenotype: Alcohol dependence<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.405<br>N cases: 9876<br>N controls: 353355"}
{"pvalue":0.3,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"All anxiety disorders","text":"Phenotype: All anxiety disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.3<br>N cases: 24662<br>N controls: 337577"}
{"pvalue":0.699,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Dementia in Alzheimer disease","text":"Phenotype: Dementia in Alzheimer disease<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.699<br>N cases: 5422<br>N controls: 356660"}
{"pvalue":0.235,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Anankastic personality disorder","text":"Phenotype: Anankastic personality disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.235<br>N cases: 1032<br>N controls: 366637"}
{"pvalue":0.487,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Anorexia (incl.atypical)","text":"Phenotype: Anorexia (incl.atypical)<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.487<br>N cases: 1897<br>N controls: 366876"}
{"pvalue":0.711,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Other anxiety disorders","text":"Phenotype: Other anxiety disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.711<br>N cases: 16887<br>N controls: 337577"}
{"pvalue":0.665,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Anxious personality disorder","text":"Phenotype: Anxious personality disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.665<br>N cases: 534<br>N controls: 366637"}
{"pvalue":0.96,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Behavioural syndromes associated with physiological disturbances and physical factors","text":"Phenotype: Behavioural syndromes associated with physiological disturbances and physical factors<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.96<br>N cases: 10401<br>N controls: 366876"}
{"pvalue":0.356,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Behavioural and emotional disorders with onset usually occurring in childhood and adolescence","text":"Phenotype: Behavioural and emotional disorders with onset usually occurring in childhood and adolescence<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.356<br>N cases: 6160<br>N controls: 371117"}
{"pvalue":0.185,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Bipolar affective disorders","text":"Phenotype: Bipolar affective disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.185<br>N cases: 7006<br>N controls: 329192"}
{"pvalue":0.175,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Bulimia nervosa (incl. atypical)","text":"Phenotype: Bulimia nervosa (incl. atypical)<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.175<br>N cases: 1028<br>N controls: 366876"}
{"pvalue":0.299,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mental and behavioural disorders due to cannabinoids","text":"Phenotype: Mental and behavioural disorders due to cannabinoids<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.299<br>N cases: 939<br>N controls: 370672"}
{"pvalue":0.00432,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Delirium, not induced by alcohol and other psychoactive substances","text":"Phenotype: Delirium, not induced by alcohol and other psychoactive substances<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00432<br>N cases: 3039<br>N controls: 356660"}
{"pvalue":0.331,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Persistent delusional disorders","text":"Phenotype: Persistent delusional disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.331<br>N cases: 2418<br>N controls: 364160"}
{"pvalue":0.107,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Dementia","text":"Phenotype: Dementia<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.107<br>N cases: 16499<br>N controls: 356660"}
{"pvalue":0.0572,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Dementia, including avohilmo","text":"Phenotype: Dementia, including avohilmo<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0572<br>N cases: 17901<br>N controls: 359376"}
{"pvalue":0.0742,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Dementia in other diseases classified elsewhere","text":"Phenotype: Dementia in other diseases classified elsewhere<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0742<br>N cases: 1157<br>N controls: 356660"}
{"pvalue":0.0189,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Unspecified dementia","text":"Phenotype: Unspecified dementia<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0189<br>N cases: 3994<br>N controls: 356660"}
{"pvalue":0.882,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Dependent personality disorder","text":"Phenotype: Dependent personality disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.882<br>N cases: 610<br>N controls: 366637"}
{"pvalue":0.918,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Depression","text":"Phenotype: Depression<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.918<br>N cases: 43280<br>N controls: 329192"}
{"pvalue":0.593,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Depression or dysthymia","text":"Phenotype: Depression or dysthymia<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.593<br>N cases: 48847<br>N controls: 225483"}
{"pvalue":0.734,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Psychotic depression","text":"Phenotype: Psychotic depression<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.734<br>N cases: 1938<br>N controls: 228968"}
{"pvalue":0.687,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Recurrent or chronic depression","text":"Phenotype: Recurrent or chronic depression<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.687<br>N cases: 17227<br>N controls: 228647"}
{"pvalue":0.762,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Dissocial personality disorder","text":"Phenotype: Dissocial personality disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.762<br>N cases: 467<br>N controls: 366637"}
{"pvalue":0.193,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Dissociative [conversion] disorders","text":"Phenotype: Dissociative [conversion] disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.193<br>N cases: 1145<br>N controls: 337577"}
{"pvalue":0.184,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Other eating disorders","text":"Phenotype: Other eating disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.184<br>N cases: 1551<br>N controls: 366876"}
{"pvalue":0.462,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Emotional disorders and disorders of social functioning with onset specific to childhood","text":"Phenotype: Emotional disorders and disorders of social functioning with onset specific to childhood<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.462<br>N cases: 1620<br>N controls: 371117"}
{"pvalue":0.561,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Emotionally unstable personality disorder","text":"Phenotype: Emotionally unstable personality disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.561<br>N cases: 4183<br>N controls: 366637"}
{"pvalue":0.735,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Generalized anxiety disorder","text":"Phenotype: Generalized anxiety disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.735<br>N cases: 4666<br>N controls: 337577"}
{"pvalue":0.358,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Gender identity disorders","text":"Phenotype: Gender identity disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.358<br>N cases: 318<br>N controls: 366637"}
{"pvalue":0.49,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Habit and impulse disorders","text":"Phenotype: Habit and impulse disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.49<br>N cases: 459<br>N controls: 366637"}
{"pvalue":0.197,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mental and behavioural disorders due to hallucinogens","text":"Phenotype: Mental and behavioural disorders due to hallucinogens<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.197<br>N cases: 152<br>N controls: 370672"}
{"pvalue":0.495,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Histrionic personality disorder","text":"Phenotype: Histrionic personality disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.495<br>N cases: 142<br>N controls: 366637"}
{"pvalue":0.0116,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Hyperkinetic disorders (excl. ADHD)","text":"Phenotype: Hyperkinetic disorders (excl. ADHD)<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0116<br>N cases: 462<br>N controls: 371117"}
{"pvalue":0.389,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Hypersomnia","text":"Phenotype: Hypersomnia<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.389<br>N cases: 373<br>N controls: 371145"}
{"pvalue":0.0336,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Insomnia","text":"Phenotype: Insomnia<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0336<br>N cases: 4214<br>N controls: 371145"}
{"pvalue":0.402,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Kela-code for severe mental illness","text":"Phenotype: Kela-code for severe mental illness<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.402<br>N cases: 15451<br>N controls: 360114"}
{"pvalue":0.807,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Kela-code for behavioural disturbances in mental retardation","text":"Phenotype: Kela-code for behavioural disturbances in mental retardation<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.807<br>N cases: 225<br>N controls: 376064"}
{"pvalue":0.636,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Manic episode","text":"Phenotype: Manic episode<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.636<br>N cases: 934<br>N controls: 329192"}
{"pvalue":0.422,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mental disorders, not otherwise specified","text":"Phenotype: Mental disorders, not otherwise specified<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.422<br>N cases: 2631<br>N controls: 360114"}
{"pvalue":0.758,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Other mental disorders due to brain damage and dysfunction and to physical disease","text":"Phenotype: Other mental disorders due to brain damage and dysfunction and to physical disease<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.758<br>N cases: 3023<br>N controls: 356660"}
{"pvalue":0.535,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mild mental retardation","text":"Phenotype: Mild mental retardation<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.535<br>N cases: 733<br>N controls: 376064"}
{"pvalue":0.34,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mixed specific developmental disorders","text":"Phenotype: Mixed specific developmental disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.34<br>N cases: 595<br>N controls: 373484"}
{"pvalue":0.985,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mixed and other personality disorders","text":"Phenotype: Mixed and other personality disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.985<br>N cases: 2619<br>N controls: 366637"}
{"pvalue":0.986,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Moderate mental retardation","text":"Phenotype: Moderate mental retardation<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.986<br>N cases: 172<br>N controls: 376064"}
{"pvalue":0.574,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Mood [affective] disorders","text":"Phenotype: Mood [affective] disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.574<br>N cases: 48085<br>N controls: 329192"}
{"pvalue":0.504,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Other and unspecified mood [affective] disorders","text":"Phenotype: Other and unspecified mood [affective] disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.504<br>N cases: 2210<br>N controls: 329192"}
{"pvalue":0.372,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Other neurotic disorders","text":"Phenotype: Other neurotic disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.372<br>N cases: 1533<br>N controls: 337577"}
{"pvalue":0.591,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Obsessive-compulsive disorder","text":"Phenotype: Obsessive-compulsive disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.591<br>N cases: 1962<br>N controls: 337577"}
{"pvalue":0.516,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mental and behavioural disorders due to opioids","text":"Phenotype: Mental and behavioural disorders due to opioids<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.516<br>N cases: 1108<br>N controls: 370672"}
{"pvalue":0.716,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mental and behavioural disorders due to multiple drug use and use of multiple drugs and use of other psychoactive substances","text":"Phenotype: Mental and behavioural disorders due to multiple drug use and use of multiple drugs and use of other psychoactive substances<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.716<br>N cases: 2299<br>N controls: 370672"}
{"pvalue":0.315,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Other specified and unspecified personality disorders","text":"Phenotype: Other specified and unspecified personality disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.315<br>N cases: 3004<br>N controls: 366637"}
{"pvalue":0.922,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Other and unspecified mental retardation","text":"Phenotype: Other and unspecified mental retardation<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.922<br>N cases: 421<br>N controls: 376064"}
{"pvalue":0.162,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Panic disorder","text":"Phenotype: Panic disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.162<br>N cases: 4801<br>N controls: 337577"}
{"pvalue":0.475,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Paranoid personality disorder","text":"Phenotype: Paranoid personality disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.475<br>N cases: 559<br>N controls: 366637"}
{"pvalue":0.216,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Personality and behavioural disorders due to brain disease, damage and dysfunction","text":"Phenotype: Personality and behavioural disorders due to brain disease, damage and dysfunction<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.216<br>N cases: 417<br>N controls: 356660"}
{"pvalue":0.395,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Persistent mood disorders","text":"Phenotype: Persistent mood disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.395<br>N cases: 6756<br>N controls: 329192"}
{"pvalue":0.469,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Enduring personality changes","text":"Phenotype: Enduring personality changes<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.469<br>N cases: 115<br>N controls: 366637"}
{"pvalue":0.123,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Other and unspecified disorders of adult personality and behaviour","text":"Phenotype: Other and unspecified disorders of adult personality and behaviour<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.123<br>N cases: 162<br>N controls: 366637"}
{"pvalue":0.483,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Pervasive developmental disorders excl. Autism + Asperger","text":"Phenotype: Pervasive developmental disorders excl. Autism + Asperger<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.483<br>N cases: 289<br>N controls: 373484"}
{"pvalue":0.612,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Phobic anxiety disorders","text":"Phenotype: Phobic anxiety disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.612<br>N cases: 4303<br>N controls: 337577"}
{"pvalue":0.041,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Unspecified behavioural syndromes associated with physiological disturbances and physical factors +Physiological and behavioural factors associated with disorders of diseases classified elsewhere","text":"Phenotype: Unspecified behavioural syndromes associated with physiological disturbances and physical factors +Physiological and behavioural factors associated with disorders of diseases classified elsewhere<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.041<br>N cases: 471<br>N controls: 366876"}
{"pvalue":0.28,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Disorders of psychological development","text":"Phenotype: Disorders of psychological development<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.28<br>N cases: 3793<br>N controls: 373484"}
{"pvalue":0.554,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Other and unspecified disorders of psychological development","text":"Phenotype: Other and unspecified disorders of psychological development<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.554<br>N cases: 290<br>N controls: 373484"}
{"pvalue":0.801,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Other and unspecified nonorganic psychotic disorders","text":"Phenotype: Other and unspecified nonorganic psychotic disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.801<br>N cases: 7508<br>N controls: 364160"}
{"pvalue":0.376,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Acute and transient psychotic disorders","text":"Phenotype: Acute and transient psychotic disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.376<br>N cases: 4255<br>N controls: 364160"}
{"pvalue":0.304,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Post-traumatic stress disorder","text":"Phenotype: Post-traumatic stress disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.304<br>N cases: 2282<br>N controls: 337577"}
{"pvalue":0.272,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Schizoaffective disorder","text":"Phenotype: Schizoaffective disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.272<br>N cases: 2742<br>N controls: 364160"}
{"pvalue":0.519,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Schizotypal disorder","text":"Phenotype: Schizotypal disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.519<br>N cases: 798<br>N controls: 364160"}
{"pvalue":0.714,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Schizoid personality disorder","text":"Phenotype: Schizoid personality disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.714<br>N cases: 550<br>N controls: 366637"}
{"pvalue":0.493,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Specific development disorders of scholastic skills","text":"Phenotype: Specific development disorders of scholastic skills<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.493<br>N cases: 1148<br>N controls: 373484"}
{"pvalue":0.86,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Schizophrenia","text":"Phenotype: Schizophrenia<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.86<br>N cases: 6515<br>N controls: 364160"}
{"pvalue":0.292,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mental and behavioural disorders due to sedatives or hypnotics","text":"Phenotype: Mental and behavioural disorders due to sedatives or hypnotics<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.292<br>N cases: 2103<br>N controls: 370672"}
{"pvalue":0.156,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Sexual dysfunction","text":"Phenotype: Sexual dysfunction<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.156<br>N cases: 326<br>N controls: 366876"}
{"pvalue":0.684,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Sleep disorders, other/unspecified","text":"Phenotype: Sleep disorders, other/unspecified<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.684<br>N cases: 779<br>N controls: 371145"}
{"pvalue":0.83,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Disorder of the sleep-wake schedule","text":"Phenotype: Disorder of the sleep-wake schedule<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.83<br>N cases: 410<br>N controls: 371145"}
{"pvalue":0.402,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Social phobias","text":"Phenotype: Social phobias<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.402<br>N cases: 2482<br>N controls: 337577"}
{"pvalue":0.467,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Somatoform disorder","text":"Phenotype: Somatoform disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.467<br>N cases: 5164<br>N controls: 337577"}
{"pvalue":0.838,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Specific development disorders of speech and language","text":"Phenotype: Specific development disorders of speech and language<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.838<br>N cases: 1648<br>N controls: 373484"}
{"pvalue":0.261,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Mental and behavioural disorders due to use of other stimulants, including caffeine","text":"Phenotype: Mental and behavioural disorders due to use of other stimulants, including caffeine<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.261<br>N cases: 856<br>N controls: 370672"}
{"pvalue":0.89,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Other reaction to severe stress, and adjustment disorders","text":"Phenotype: Other reaction to severe stress, and adjustment disorders<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.89<br>N cases: 13913<br>N controls: 337577"}
{"pvalue":0.206,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Substance use, excluding alcohol","text":"Phenotype: Substance use, excluding alcohol<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.206<br>N cases: 6605<br>N controls: 353355"}
{"pvalue":0.358,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Unspecified organic or symptomatic mental disorder","text":"Phenotype: Unspecified organic or symptomatic mental disorder<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.358<br>N cases: 97<br>N controls: 356660"}
{"pvalue":0.173,"sign":-1,"group":"F5: Mental and behavioural disorders","label":"Vascular dementia","text":"Phenotype: Vascular dementia<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.173<br>N cases: 2335<br>N controls: 360778"}
{"pvalue":0.128,"sign":1,"group":"G6: Nervous system diseases","label":"Focal epilepsy","text":"Phenotype: Focal epilepsy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.128<br>N cases: 6842<br>N controls: 365537"}
{"pvalue":0.237,"sign":1,"group":"G6: Nervous system diseases","label":"Focal epilepsy, mode (most common among epilepsy diagnosis)","text":"Phenotype: Focal epilepsy, mode (most common among epilepsy diagnosis)<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.237<br>N cases: 1260<br>N controls: 365537"}
{"pvalue":0.0599,"sign":1,"group":"G6: Nervous system diseases","label":"Focal epilepsy, strict definition","text":"Phenotype: Focal epilepsy, strict definition<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0599<br>N cases: 6213<br>N controls: 365534"}
{"pvalue":0.00013,"sign":-1,"group":"I9: Circulatory system diseases","label":"Diseases of arteries, arterioles and capillaries (FINNGEN)","text":"Phenotype: Diseases of arteries, arterioles and capillaries (FINNGEN)<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.000129<br>N cases: 22224<br>N controls: 191924"}
{"pvalue":0.274,"sign":-1,"group":"G6: Nervous system diseases","label":"Alzheimer’s disease, wide definition","text":"Phenotype: Alzheimer’s disease, wide definition<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.274<br>N cases: 13393<br>N controls: 363884"}
{"pvalue":0.727,"sign":1,"group":"G6: Nervous system diseases","label":"Degeneration of the brain due to alcohol","text":"Phenotype: Degeneration of the brain due to alcohol<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.727<br>N cases: 592<br>N controls: 366632"}
{"pvalue":0.928,"sign":1,"group":"G6: Nervous system diseases","label":"Alcohol induced polyneuropathy","text":"Phenotype: Alcohol induced polyneuropathy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.928<br>N cases: 249<br>N controls: 370790"}
{"pvalue":0.543,"sign":1,"group":"G6: Nervous system diseases","label":"Motor neuron disease","text":"Phenotype: Motor neuron disease<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.543<br>N cases: 483<br>N controls: 170667"}
{"pvalue":0.725,"sign":-1,"group":"G6: Nervous system diseases","label":"Alzheimer disease","text":"Phenotype: Alzheimer disease<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.725<br>N cases: 9301<br>N controls: 367976"}
{"pvalue":0.414,"sign":-1,"group":"G6: Nervous system diseases","label":"Anoxic brain damage","text":"Phenotype: Anoxic brain damage<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.414<br>N cases: 368<br>N controls: 350251"}
{"pvalue":0.0134,"sign":-1,"group":"G6: Nervous system diseases","label":"Circumscribed brain atrophy","text":"Phenotype: Circumscribed brain atrophy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0134<br>N cases: 467<br>N controls: 366632"}
{"pvalue":0.722,"sign":-1,"group":"G6: Nervous system diseases","label":"Atypical facial pain","text":"Phenotype: Atypical facial pain<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.722<br>N cases: 1372<br>N controls: 330377"}
{"pvalue":0.9,"sign":1,"group":"G6: Nervous system diseases","label":"Autonomic disorders","text":"Phenotype: Autonomic disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.9<br>N cases: 549<br>N controls: 350251"}
{"pvalue":0.0903,"sign":-1,"group":"G6: Nervous system diseases","label":"Other degenerative diseases of the basal ganglia","text":"Phenotype: Other degenerative diseases of the basal ganglia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0903<br>N cases: 296<br>N controls: 367444"}
{"pvalue":0.466,"sign":-1,"group":"G6: Nervous system diseases","label":"Bell's palsy","text":"Phenotype: Bell's palsy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.466<br>N cases: 3453<br>N controls: 330377"}
{"pvalue":0.21,"sign":-1,"group":"G6: Nervous system diseases","label":"Benign intracranial hypertension","text":"Phenotype: Benign intracranial hypertension<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.21<br>N cases: 231<br>N controls: 350251"}
{"pvalue":0.31,"sign":1,"group":"G6: Nervous system diseases","label":"Brachial plexus disorders","text":"Phenotype: Brachial plexus disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.31<br>N cases: 2757<br>N controls: 330377"}
{"pvalue":0.0131,"sign":1,"group":"G6: Nervous system diseases","label":"Carpal tunnel syndrome","text":"Phenotype: Carpal tunnel syndrome<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0131<br>N cases: 22426<br>N controls: 330377"}
{"pvalue":0.444,"sign":1,"group":"G6: Nervous system diseases","label":"Cauda equina syndrome","text":"Phenotype: Cauda equina syndrome<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.444<br>N cases: 290<br>N controls: 373780"}
{"pvalue":0.89,"sign":1,"group":"G6: Nervous system diseases","label":"Causalgia","text":"Phenotype: Causalgia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.89<br>N cases: 438<br>N controls: 330377"}
{"pvalue":0.0953,"sign":-1,"group":"G6: Nervous system diseases","label":"Cerebral cysts","text":"Phenotype: Cerebral cysts<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0953<br>N cases: 1567<br>N controls: 350251"}
{"pvalue":0.682,"sign":1,"group":"G6: Nervous system diseases","label":"Cervical root disorders","text":"Phenotype: Cervical root disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.682<br>N cases: 190<br>N controls: 330377"}
{"pvalue":0.14,"sign":-1,"group":"G6: Nervous system diseases","label":"Cluster headache, strict, including avohilmo","text":"Phenotype: Cluster headache, strict, including avohilmo<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.14<br>N cases: 1297<br>N controls: 375980"}
{"pvalue":0.0828,"sign":-1,"group":"G6: Nervous system diseases","label":"Cluster headache, wide","text":"Phenotype: Cluster headache, wide<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0828<br>N cases: 1107<br>N controls: 287837"}
{"pvalue":0.81,"sign":1,"group":"G6: Nervous system diseases","label":"Intracranial and intraspinal abscess and granuloma","text":"Phenotype: Intracranial and intraspinal abscess and granuloma<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.81<br>N cases: 283<br>N controls: 374844"}
{"pvalue":0.668,"sign":-1,"group":"G6: Nervous system diseases","label":"Other disorders of central nervous system","text":"Phenotype: Other disorders of central nervous system<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.668<br>N cases: 285<br>N controls: 350251"}
{"pvalue":0.63,"sign":-1,"group":"G6: Nervous system diseases","label":"Cerebral palsy and other paralytic syndromes","text":"Phenotype: Cerebral palsy and other paralytic syndromes<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.63<br>N cases: 3497<br>N controls: 373780"}
{"pvalue":0.16,"sign":-1,"group":"G6: Nervous system diseases","label":"Cerebral palsy","text":"Phenotype: Cerebral palsy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.16<br>N cases: 482<br>N controls: 373780"}
{"pvalue":0.791,"sign":-1,"group":"G6: Nervous system diseases","label":"Other and unspecified degenerative diseases of nervous system","text":"Phenotype: Other and unspecified degenerative diseases of nervous system<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.791<br>N cases: 545<br>N controls: 366632"}
{"pvalue":0.757,"sign":1,"group":"G6: Nervous system diseases","label":"Senile degeneration of the brain, not elsewhere classified","text":"Phenotype: Senile degeneration of the brain, not elsewhere classified<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.757<br>N cases: 107<br>N controls: 366632"}
{"pvalue":0.348,"sign":-1,"group":"G6: Nervous system diseases","label":"Disorders of brain, other and unspecified","text":"Phenotype: Disorders of brain, other and unspecified<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.348<br>N cases: 266<br>N controls: 350251"}
{"pvalue":0.788,"sign":1,"group":"G6: Nervous system diseases","label":"Disorders of other and unspecified cranial nerves","text":"Phenotype: Disorders of other and unspecified cranial nerves<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.788<br>N cases: 142<br>N controls: 330377"}
{"pvalue":0.796,"sign":1,"group":"G6: Nervous system diseases","label":"Other acute disseminated demyelination","text":"Phenotype: Other acute disseminated demyelination<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.796<br>N cases: 277<br>N controls: 374678"}
{"pvalue":0.795,"sign":1,"group":"G6: Nervous system diseases","label":"Drug-induced polyneuropathy","text":"Phenotype: Drug-induced polyneuropathy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.795<br>N cases: 208<br>N controls: 370790"}
{"pvalue":0.164,"sign":1,"group":"G6: Nervous system diseases","label":"Dystonia","text":"Phenotype: Dystonia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.164<br>N cases: 1500<br>N controls: 367444"}
{"pvalue":0.288,"sign":-1,"group":"G6: Nervous system diseases","label":"Encephalopathy","text":"Phenotype: Encephalopathy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.288<br>N cases: 249<br>N controls: 350251"}
{"pvalue":0.581,"sign":-1,"group":"G6: Nervous system diseases","label":"Other encephalitis","text":"Phenotype: Other encephalitis<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.581<br>N cases: 705<br>N controls: 374844"}
{"pvalue":0.00722,"sign":1,"group":"G6: Nervous system diseases","label":"Episodal and paroxysmal disorders","text":"Phenotype: Episodal and paroxysmal disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00722<br>N cases: 89440<br>N controls: 287837"}
{"pvalue":0.0254,"sign":1,"group":"G6: Nervous system diseases","label":"Epilepsy","text":"Phenotype: Epilepsy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0254<br>N cases: 11740<br>N controls: 287837"}
{"pvalue":0.0566,"sign":1,"group":"G6: Nervous system diseases","label":"Other facial nerve disorders","text":"Phenotype: Other facial nerve disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0566<br>N cases: 756<br>N controls: 330377"}
{"pvalue":0.314,"sign":1,"group":"G6: Nervous system diseases","label":"Lesion of lateral popliteal nerve","text":"Phenotype: Lesion of lateral popliteal nerve<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.314<br>N cases: 1288<br>N controls: 330377"}
{"pvalue":0.0217,"sign":1,"group":"G6: Nervous system diseases","label":"Lesion of femoral nerve","text":"Phenotype: Lesion of femoral nerve<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0217<br>N cases: 208<br>N controls: 330377"}
{"pvalue":0.872,"sign":1,"group":"G6: Nervous system diseases","label":"Lesion of medial popliteal nerve","text":"Phenotype: Lesion of medial popliteal nerve<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.872<br>N cases: 92<br>N controls: 330377"}
{"pvalue":0.741,"sign":-1,"group":"G6: Nervous system diseases","label":"Guillain-Barre syndrome","text":"Phenotype: Guillain-Barre syndrome<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.741<br>N cases: 415<br>N controls: 370790"}
{"pvalue":0.846,"sign":-1,"group":"G6: Nervous system diseases","label":"Communicating hydrocephalus","text":"Phenotype: Communicating hydrocephalus<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.846<br>N cases: 488<br>N controls: 375610"}
{"pvalue":0.163,"sign":1,"group":"G6: Nervous system diseases","label":"Hydrocephalus in other diseases","text":"Phenotype: Hydrocephalus in other diseases<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.163<br>N cases: 145<br>N controls: 375610"}
{"pvalue":0.805,"sign":-1,"group":"G6: Nervous system diseases","label":"Normal-pressure hydrocephalus","text":"Phenotype: Normal-pressure hydrocephalus<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.805<br>N cases: 767<br>N controls: 375610"}
{"pvalue":0.898,"sign":1,"group":"G6: Nervous system diseases","label":"Obstructive hydrocephalus","text":"Phenotype: Obstructive hydrocephalus<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.898<br>N cases: 369<br>N controls: 375610"}
{"pvalue":0.792,"sign":1,"group":"G6: Nervous system diseases","label":"Other and unspecified hydrocephalus","text":"Phenotype: Other and unspecified hydrocephalus<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.792<br>N cases: 393<br>N controls: 375610"}
{"pvalue":0.00827,"sign":1,"group":"G6: Nervous system diseases","label":"Other headache syndromes","text":"Phenotype: Other headache syndromes<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00827<br>N cases: 15851<br>N controls: 287837"}
{"pvalue":0.227,"sign":1,"group":"G6: Nervous system diseases","label":"Hemiplegia","text":"Phenotype: Hemiplegia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.227<br>N cases: 1537<br>N controls: 373780"}
{"pvalue":0.643,"sign":1,"group":"G6: Nervous system diseases","label":"Hereditary ataxia","text":"Phenotype: Hereditary ataxia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.643<br>N cases: 339<br>N controls: 376185"}
{"pvalue":0.622,"sign":-1,"group":"G6: Nervous system diseases","label":"Hereditary motor and sensory neuropathy","text":"Phenotype: Hereditary motor and sensory neuropathy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.622<br>N cases: 218<br>N controls: 370790"}
{"pvalue":0.266,"sign":1,"group":"G6: Nervous system diseases","label":"Other and unspecified neuropathies","text":"Phenotype: Other and unspecified neuropathies<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.266<br>N cases: 112<br>N controls: 370790"}
{"pvalue":0.384,"sign":-1,"group":"G6: Nervous system diseases","label":"Horner syndrome","text":"Phenotype: Horner syndrome<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.384<br>N cases: 309<br>N controls: 376728"}
{"pvalue":0.631,"sign":1,"group":"G6: Nervous system diseases","label":"Hydrocephalus","text":"Phenotype: Hydrocephalus<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.631<br>N cases: 1667<br>N controls: 350251"}
{"pvalue":0.644,"sign":-1,"group":"G6: Nervous system diseases","label":"Intercostal neuropathy","text":"Phenotype: Intercostal neuropathy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.644<br>N cases: 207<br>N controls: 330377"}
{"pvalue":0.155,"sign":1,"group":"G6: Nervous system diseases","label":"Idiopathic peripheral autonomic neuropathy","text":"Phenotype: Idiopathic peripheral autonomic neuropathy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.155<br>N cases: 89<br>N controls: 376728"}
{"pvalue":0.723,"sign":-1,"group":"G6: Nervous system diseases","label":"Lumbosacral plexus disorders","text":"Phenotype: Lumbosacral plexus disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.723<br>N cases: 88<br>N controls: 330377"}
{"pvalue":0.843,"sign":-1,"group":"G6: Nervous system diseases","label":"Lumbosacral root disorders, not elsewhere classified","text":"Phenotype: Lumbosacral root disorders, not elsewhere classified<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.843<br>N cases: 353<br>N controls: 330377"}
{"pvalue":0.0525,"sign":1,"group":"G6: Nervous system diseases","label":"Other lesions of median nerve","text":"Phenotype: Other lesions of median nerve<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0525<br>N cases: 732<br>N controls: 330377"}
{"pvalue":0.629,"sign":1,"group":"G6: Nervous system diseases","label":"Bacterial meningitis","text":"Phenotype: Bacterial meningitis<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.629<br>N cases: 971<br>N controls: 374844"}
{"pvalue":0.809,"sign":-1,"group":"G6: Nervous system diseases","label":"Other meningitis","text":"Phenotype: Other meningitis<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.809<br>N cases: 411<br>N controls: 374844"}
{"pvalue":0.447,"sign":-1,"group":"G6: Nervous system diseases","label":"Viral meningitis","text":"Phenotype: Viral meningitis<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.447<br>N cases: 102<br>N controls: 374844"}
{"pvalue":0.11,"sign":-1,"group":"G6: Nervous system diseases","label":"Meralgia paraesthetica","text":"Phenotype: Meralgia paraesthetica<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.11<br>N cases: 849<br>N controls: 330377"}
{"pvalue":0.00178,"sign":1,"group":"G6: Nervous system diseases","label":"Migraine","text":"Phenotype: Migraine<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00178<br>N cases: 18477<br>N controls: 287837"}
{"pvalue":0.626,"sign":1,"group":"G6: Nervous system diseases","label":"Migraine without aura, drug-induced","text":"Phenotype: Migraine without aura, drug-induced<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.626<br>N cases: 321<br>N controls: 376956"}
{"pvalue":0.133,"sign":1,"group":"G6: Nervous system diseases","label":"Migraine without aura","text":"Phenotype: Migraine without aura<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.133<br>N cases: 6730<br>N controls: 287837"}
{"pvalue":0.183,"sign":1,"group":"G6: Nervous system diseases","label":"Migraine without aura and triptan purchases","text":"Phenotype: Migraine without aura and triptan purchases<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.183<br>N cases: 4989<br>N controls: 337890"}
{"pvalue":0.916,"sign":1,"group":"G6: Nervous system diseases","label":"Migraine with aura, drug-induced","text":"Phenotype: Migraine with aura, drug-induced<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.916<br>N cases: 307<br>N controls: 376970"}
{"pvalue":0.00909,"sign":1,"group":"G6: Nervous system diseases","label":"Migraine with aura","text":"Phenotype: Migraine with aura<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00909<br>N cases: 7917<br>N controls: 287837"}
{"pvalue":0.229,"sign":1,"group":"G6: Nervous system diseases","label":"Migraine with aura and triptan purchases","text":"Phenotype: Migraine with aura and triptan purchases<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.229<br>N cases: 4503<br>N controls: 337890"}
{"pvalue":0.555,"sign":1,"group":"G6: Nervous system diseases","label":"Mitochondrial myopathy","text":"Phenotype: Mitochondrial myopathy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.555<br>N cases: 98<br>N controls: 373848"}
{"pvalue":0.768,"sign":-1,"group":"G6: Nervous system diseases","label":"Other and unspecified mononeuropathies of lower limb","text":"Phenotype: Other and unspecified mononeuropathies of lower limb<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.768<br>N cases: 778<br>N controls: 330377"}
{"pvalue":0.851,"sign":1,"group":"G6: Nervous system diseases","label":"Other and unspecified mononeuropathies of upper limb","text":"Phenotype: Other and unspecified mononeuropathies of upper limb<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.851<br>N cases: 798<br>N controls: 330377"}
{"pvalue":0.602,"sign":-1,"group":"G6: Nervous system diseases","label":"Other and unspecified mononeuropathies, also in other diseases","text":"Phenotype: Other and unspecified mononeuropathies, also in other diseases<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.602<br>N cases: 874<br>N controls: 330377"}
{"pvalue":0.252,"sign":-1,"group":"G6: Nervous system diseases","label":"Monoplegia","text":"Phenotype: Monoplegia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.252<br>N cases: 385<br>N controls: 373780"}
{"pvalue":0.865,"sign":1,"group":"G6: Nervous system diseases","label":"MS-disease / Multiple Sclerosis","text":"Phenotype: MS-disease / Multiple Sclerosis<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.865<br>N cases: 2182<br>N controls: 373987"}
{"pvalue":0.453,"sign":1,"group":"G6: Nervous system diseases","label":"Other and unspecified primary disorders of muscles","text":"Phenotype: Other and unspecified primary disorders of muscles<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.453<br>N cases: 195<br>N controls: 373848"}
{"pvalue":0.636,"sign":-1,"group":"G6: Nervous system diseases","label":"Muscular dystrophy","text":"Phenotype: Muscular dystrophy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.636<br>N cases: 210<br>N controls: 373848"}
{"pvalue":0.412,"sign":1,"group":"G6: Nervous system diseases","label":"Myasthenia gravis","text":"Phenotype: Myasthenia gravis<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.412<br>N cases: 426<br>N controls: 373848"}
{"pvalue":0.506,"sign":-1,"group":"G6: Nervous system diseases","label":"Disorders of myoneural junction and muscle in diseases classified elsewhere","text":"Phenotype: Disorders of myoneural junction and muscle in diseases classified elsewhere<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.506<br>N cases: 200<br>N controls: 373848"}
{"pvalue":0.428,"sign":1,"group":"G6: Nervous system diseases","label":"Diseases of the myoneural junction and muscle","text":"Phenotype: Diseases of the myoneural junction and muscle<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.428<br>N cases: 3429<br>N controls: 373848"}
{"pvalue":0.894,"sign":1,"group":"G6: Nervous system diseases","label":"Other and unspecified myoneural disorders","text":"Phenotype: Other and unspecified myoneural disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.894<br>N cases: 98<br>N controls: 373848"}
{"pvalue":0.607,"sign":1,"group":"G6: Nervous system diseases","label":"Other and unspecified myopathies","text":"Phenotype: Other and unspecified myopathies<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.607<br>N cases: 2313<br>N controls: 373848"}
{"pvalue":0.319,"sign":1,"group":"G6: Nervous system diseases","label":"Myotonic disorders","text":"Phenotype: Myotonic disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.319<br>N cases: 206<br>N controls: 373848"}
{"pvalue":0.142,"sign":1,"group":"G6: Nervous system diseases","label":"Narcolepsy and cataplexy","text":"Phenotype: Narcolepsy and cataplexy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.142<br>N cases: 176<br>N controls: 287837"}
{"pvalue":0.169,"sign":1,"group":"G6: Nervous system diseases","label":"Nerve, nerve root and plexus disorders","text":"Phenotype: Nerve, nerve root and plexus disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.169<br>N cases: 46900<br>N controls: 330377"}
{"pvalue":0.777,"sign":-1,"group":"G6: Nervous system diseases","label":"Systemic atrophies primarily affecting the central nervous system","text":"Phenotype: Systemic atrophies primarily affecting the central nervous system<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.777<br>N cases: 1092<br>N controls: 376185"}
{"pvalue":0.781,"sign":-1,"group":"G6: Nervous system diseases","label":"Inflammatory diseases of the central nervous system","text":"Phenotype: Inflammatory diseases of the central nervous system<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.781<br>N cases: 2433<br>N controls: 374844"}
{"pvalue":0.535,"sign":1,"group":"G6: Nervous system diseases","label":"Other disorders of nervous system","text":"Phenotype: Other disorders of nervous system<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.535<br>N cases: 1754<br>N controls: 350251"}
{"pvalue":0.736,"sign":1,"group":"G6: Nervous system diseases","label":"Other demyelinating diseases of the central nervous system","text":"Phenotype: Other demyelinating diseases of the central nervous system<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.736<br>N cases: 1029<br>N controls: 374678"}
{"pvalue":0.913,"sign":-1,"group":"G6: Nervous system diseases","label":"Other neurological diseases","text":"Phenotype: Other neurological diseases<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.913<br>N cases: 27026<br>N controls: 350251"}
{"pvalue":0.289,"sign":-1,"group":"G6: Nervous system diseases","label":"Other and unspecified paralytic syndromes","text":"Phenotype: Other and unspecified paralytic syndromes<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.289<br>N cases: 359<br>N controls: 373780"}
{"pvalue":0.135,"sign":-1,"group":"G6: Nervous system diseases","label":"Paraplegia, diplegia of upper limbs","text":"Phenotype: Paraplegia, diplegia of upper limbs<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.135<br>N cases: 594<br>N controls: 373780"}
{"pvalue":0.123,"sign":-1,"group":"G6: Nervous system diseases","label":"Parkinson's disease","text":"Phenotype: Parkinson's disease<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.123<br>N cases: 4235<br>N controls: 373042"}
{"pvalue":0.0205,"sign":1,"group":"G6: Nervous system diseases","label":"Other disorders of peripheral nervous system","text":"Phenotype: Other disorders of peripheral nervous system<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0205<br>N cases: 143<br>N controls: 370790"}
{"pvalue":0.17,"sign":-1,"group":"G6: Nervous system diseases","label":"Lesion of plantar nerve","text":"Phenotype: Lesion of plantar nerve<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.17<br>N cases: 1784<br>N controls: 330377"}
{"pvalue":0.602,"sign":-1,"group":"G6: Nervous system diseases","label":"Other and unspecified polyneuropathies, also in other diseases","text":"Phenotype: Other and unspecified polyneuropathies, also in other diseases<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.602<br>N cases: 5553<br>N controls: 370790"}
{"pvalue":0.37,"sign":1,"group":"G6: Nervous system diseases","label":"Postprocedural disorders of nervous system","text":"Phenotype: Postprocedural disorders of nervous system<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.37<br>N cases: 2146<br>N controls: 350251"}
{"pvalue":0.225,"sign":-1,"group":"G6: Nervous system diseases","label":"Postviral fatigue syndrome","text":"Phenotype: Postviral fatigue syndrome<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.225<br>N cases: 169<br>N controls: 350251"}
{"pvalue":0.587,"sign":1,"group":"G6: Nervous system diseases","label":"Postzoster neuralgia","text":"Phenotype: Postzoster neuralgia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.587<br>N cases: 313<br>N controls: 330377"}
{"pvalue":0.211,"sign":-1,"group":"G6: Nervous system diseases","label":"Lesion of radial nerve","text":"Phenotype: Lesion of radial nerve<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.211<br>N cases: 1033<br>N controls: 330377"}
{"pvalue":0.178,"sign":1,"group":"G6: Nervous system diseases","label":"Other and unspecified nerve root and plexus disorders, also in other diseases","text":"Phenotype: Other and unspecified nerve root and plexus disorders, also in other diseases<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.178<br>N cases: 5294<br>N controls: 330377"}
{"pvalue":0.667,"sign":-1,"group":"G6: Nervous system diseases","label":"Lesion of sciatic nerve","text":"Phenotype: Lesion of sciatic nerve<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.667<br>N cases: 1367<br>N controls: 330377"}
{"pvalue":0.597,"sign":1,"group":"G6: Nervous system diseases","label":"Sleep apnoea","text":"Phenotype: Sleep apnoea<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.597<br>N cases: 38998<br>N controls: 336659"}
{"pvalue":0.453,"sign":1,"group":"G6: Nervous system diseases","label":"Sleep apnoea, including avohilmo","text":"Phenotype: Sleep apnoea, including avohilmo<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.453<br>N cases: 41704<br>N controls: 335573"}
{"pvalue":0.657,"sign":1,"group":"G6: Nervous system diseases","label":"Other sleep disorders","text":"Phenotype: Other sleep disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.657<br>N cases: 3219<br>N controls: 287837"}
{"pvalue":0.897,"sign":-1,"group":"G6: Nervous system diseases","label":"Other and unspecified spinal muscular atrophies","text":"Phenotype: Other and unspecified spinal muscular atrophies<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.897<br>N cases: 219<br>N controls: 376185"}
{"pvalue":0.706,"sign":1,"group":"G6: Nervous system diseases","label":"Other diseases of spinal cord","text":"Phenotype: Other diseases of spinal cord<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.706<br>N cases: 804<br>N controls: 350251"}
{"pvalue":0.791,"sign":-1,"group":"G6: Nervous system diseases","label":"Status epilepticus","text":"Phenotype: Status epilepticus<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.791<br>N cases: 1023<br>N controls: 287837"}
{"pvalue":0.0642,"sign":-1,"group":"G6: Nervous system diseases","label":"Tarsal tunnel syndrome","text":"Phenotype: Tarsal tunnel syndrome<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0642<br>N cases: 251<br>N controls: 330377"}
{"pvalue":0.168,"sign":-1,"group":"G6: Nervous system diseases","label":"Tetraplegia","text":"Phenotype: Tetraplegia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.168<br>N cases: 182<br>N controls: 373780"}
{"pvalue":0.722,"sign":1,"group":"G6: Nervous system diseases","label":"Trigeminal neuralgia","text":"Phenotype: Trigeminal neuralgia<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.722<br>N cases: 1599<br>N controls: 330377"}
{"pvalue":0.739,"sign":1,"group":"G6: Nervous system diseases","label":"Other and unspecified trigeminal disorders","text":"Phenotype: Other and unspecified trigeminal disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.739<br>N cases: 409<br>N controls: 330377"}
{"pvalue":0.562,"sign":1,"group":"G6: Nervous system diseases","label":"Lesion of ulnar nerve","text":"Phenotype: Lesion of ulnar nerve<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.562<br>N cases: 4151<br>N controls: 330377"}
{"pvalue":0.486,"sign":-1,"group":"G6: Nervous system diseases","label":"Extrapyramidal and movement disorders","text":"Phenotype: Extrapyramidal and movement disorders<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.486<br>N cases: 9833<br>N controls: 367444"}
{"pvalue":0.978,"sign":-1,"group":"G6: Nervous system diseases","label":"Other extrapyramidal and movement disorders in other diseases","text":"Phenotype: Other extrapyramidal and movement disorders in other diseases<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.978<br>N cases: 4594<br>N controls: 367444"}
{"pvalue":0.492,"sign":-1,"group":"G6: Nervous system diseases","label":"Generalized epilepsy","text":"Phenotype: Generalized epilepsy<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.492<br>N cases: 1298<br>N controls: 365534"}
{"pvalue":0.445,"sign":1,"group":"G6: Nervous system diseases","label":"Generalized epilepsy, mode (most common among epilepsy diagnosis)","text":"Phenotype: Generalized epilepsy, mode (most common among epilepsy diagnosis)<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.445<br>N cases: 2235<br>N controls: 365537"}
{"pvalue":0.227,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Generalized skin eruption due to drugs and medicaments","text":"Phenotype: Generalized skin eruption due to drugs and medicaments<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.227<br>N cases: 1051<br>N controls: 376226"}
{"pvalue":0.938,"sign":1,"group":"G6: Nervous system diseases","label":"Generalized epilepsy, strict definition","text":"Phenotype: Generalized epilepsy, strict definition<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.938<br>N cases: 669<br>N controls: 365534"}
{"pvalue":0.575,"sign":1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Graves ophthalmopathy","text":"Phenotype: Graves ophthalmopathy<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.575<br>N cases: 643<br>N controls: 376634"}
{"pvalue":0.00016,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Allergic conjunctivitis","text":"Phenotype: Allergic conjunctivitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.000155<br>N cases: 20958<br>N controls: 356319"}
{"pvalue":0.975,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Amblyopia ex anopsia","text":"Phenotype: Amblyopia ex anopsia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.975<br>N cases: 1046<br>N controls: 360091"}
{"pvalue":0.902,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Age-related macular degeneration (whether dry or wet)","text":"Phenotype: Age-related macular degeneration (whether dry or wet)<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.902<br>N cases: 8913<br>N controls: 348936"}
{"pvalue":0.963,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Anisometropia and aniseikonia","text":"Phenotype: Anisometropia and aniseikonia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.963<br>N cases: 793<br>N controls: 361237"}
{"pvalue":0.519,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Anomalies of pupillary function","text":"Phenotype: Anomalies of pupillary function<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.519<br>N cases: 509<br>N controls: 373254"}
{"pvalue":0.877,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Aphakia","text":"Phenotype: Aphakia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.877<br>N cases: 471<br>N controls: 312864"}
{"pvalue":0.132,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Astigmatism","text":"Phenotype: Astigmatism<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.132<br>N cases: 1502<br>N controls: 361237"}
{"pvalue":0.905,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Background retinopathy and retinal vascular changes","text":"Phenotype: Background retinopathy and retinal vascular changes<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.905<br>N cases: 533<br>N controls: 344569"}
{"pvalue":0.507,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other and unspecified disorders of binocular movement","text":"Phenotype: Other and unspecified disorders of binocular movement<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.507<br>N cases: 135<br>N controls: 361237"}
{"pvalue":0.747,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of binocular movement","text":"Phenotype: Other disorders of binocular movement<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.747<br>N cases: 581<br>N controls: 361237"}
{"pvalue":0.135,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of binocular vision","text":"Phenotype: Other disorders of binocular vision<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.135<br>N cases: 327<br>N controls: 360091"}
{"pvalue":0.634,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Blepharochalasis","text":"Phenotype: Blepharochalasis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.634<br>N cases: 8547<br>N controls: 344684"}
{"pvalue":0.762,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Visual impairment including blindness (binocular or monocular)","text":"Phenotype: Visual impairment including blindness (binocular or monocular)<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.762<br>N cases: 1882<br>N controls: 360091"}
{"pvalue":0.224,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Blindness, monocular","text":"Phenotype: Blindness, monocular<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.224<br>N cases: 223<br>N controls: 360091"}
{"pvalue":0.112,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Bullous keratopathy","text":"Phenotype: Bullous keratopathy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.112<br>N cases: 200<br>N controls: 357814"}
{"pvalue":0.405,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other cataract","text":"Phenotype: Other cataract<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.405<br>N cases: 17699<br>N controls: 312864"}
{"pvalue":0.317,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Senile cataract","text":"Phenotype: Senile cataract<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.317<br>N cases: 59522<br>N controls: 312864"}
{"pvalue":0.281,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Central retinal artery occlusion","text":"Phenotype: Central retinal artery occlusion<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.281<br>N cases: 546<br>N controls: 344569"}
{"pvalue":0.332,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Chalazion","text":"Phenotype: Chalazion<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.332<br>N cases: 3389<br>N controls: 344684"}
{"pvalue":0.849,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Choroidal haemorrhage and rupture","text":"Phenotype: Choroidal haemorrhage and rupture<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.849<br>N cases: 80<br>N controls: 344569"}
{"pvalue":0.864,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Chorioretinal inflammation","text":"Phenotype: Chorioretinal inflammation<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.864<br>N cases: 761<br>N controls: 344569"}
{"pvalue":0.0918,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other specified and unspecified disorders of choroid","text":"Phenotype: Other specified and unspecified disorders of choroid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0918<br>N cases: 95<br>N controls: 344569"}
{"pvalue":0.126,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of choroid","text":"Phenotype: Other disorders of choroid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.126<br>N cases: 358<br>N controls: 344569"}
{"pvalue":0.72,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Disorders of choroid and retina","text":"Phenotype: Disorders of choroid and retina<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.72<br>N cases: 32708<br>N controls: 344569"}
{"pvalue":0.213,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Chorioretinal scars","text":"Phenotype: Chorioretinal scars<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.213<br>N cases: 82<br>N controls: 344569"}
{"pvalue":0.238,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"conjunctival haemorrhage","text":"Phenotype: conjunctival haemorrhage<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.238<br>N cases: 1861<br>N controls: 345122"}
{"pvalue":0.407,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other specified and unspecified disorders of conjunctiva","text":"Phenotype: Other specified and unspecified disorders of conjunctiva<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.407<br>N cases: 219<br>N controls: 345122"}
{"pvalue":0.684,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"conjunctival degenerations and deposits","text":"Phenotype: conjunctival degenerations and deposits<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.684<br>N cases: 575<br>N controls: 345122"}
{"pvalue":0.0172,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Conjunctivitis (acute, non atopic)","text":"Phenotype: Conjunctivitis (acute, non atopic)<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0172<br>N cases: 8907<br>N controls: 345122"}
{"pvalue":0.0199,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Atopic conjunctivitis","text":"Phenotype: Atopic conjunctivitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0199<br>N cases: 1211<br>N controls: 345122"}
{"pvalue":0.0291,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Chronic conjunctivitis","text":"Phenotype: Chronic conjunctivitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0291<br>N cases: 782<br>N controls: 345122"}
{"pvalue":0.00005,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Conjunctivitis","text":"Phenotype: Conjunctivitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 4.58e-05<br>N cases: 28895<br>N controls: 345122"}
{"pvalue":0.943,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other conjunctival vascular disorders and cysts","text":"Phenotype: Other conjunctival vascular disorders and cysts<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.943<br>N cases: 585<br>N controls: 345122"}
{"pvalue":0.253,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Convergence insufficiency and excess","text":"Phenotype: Convergence insufficiency and excess<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.253<br>N cases: 342<br>N controls: 361237"}
{"pvalue":0.0454,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Convergent concomitant strabismus","text":"Phenotype: Convergent concomitant strabismus<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0454<br>N cases: 1690<br>N controls: 361237"}
{"pvalue":0.947,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Keratoconus","text":"Phenotype: Keratoconus<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.947<br>N cases: 625<br>N controls: 357814"}
{"pvalue":0.359,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Corneal degeneration","text":"Phenotype: Corneal degeneration<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.359<br>N cases: 297<br>N controls: 357814"}
{"pvalue":0.111,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other and unspecified corneal deformities and disorders","text":"Phenotype: Other and unspecified corneal deformities and disorders<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.111<br>N cases: 832<br>N controls: 357814"}
{"pvalue":0.594,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other corneal oedema","text":"Phenotype: Other corneal oedema<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.594<br>N cases: 164<br>N controls: 357814"}
{"pvalue":0.0548,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of cornea","text":"Phenotype: Other disorders of cornea<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0548<br>N cases: 2510<br>N controls: 357814"}
{"pvalue":0.593,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Corneal scars and opacities","text":"Phenotype: Corneal scars and opacities<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.593<br>N cases: 616<br>N controls: 357814"}
{"pvalue":0.177,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Corneal pigmentations and deposits","text":"Phenotype: Corneal pigmentations and deposits<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.177<br>N cases: 102<br>N controls: 357814"}
{"pvalue":0.571,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Corneal ulcer","text":"Phenotype: Corneal ulcer<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.571<br>N cases: 5476<br>N controls: 357814"}
{"pvalue":0.621,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Colour vision deficiencies","text":"Phenotype: Colour vision deficiencies<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.621<br>N cases: 109<br>N controls: 360091"}
{"pvalue":0.534,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Dacryoadenitis","text":"Phenotype: Dacryoadenitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.534<br>N cases: 198<br>N controls: 344684"}
{"pvalue":0.639,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Degenerative myopia","text":"Phenotype: Degenerative myopia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.639<br>N cases: 161<br>N controls: 361552"}
{"pvalue":0.0805,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Diplopia","text":"Phenotype: Diplopia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0805<br>N cases: 3700<br>N controls: 360091"}
{"pvalue":0.419,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other specified and unspecified disorders of lens","text":"Phenotype: Other specified and unspecified disorders of lens<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.419<br>N cases: 215<br>N controls: 312864"}
{"pvalue":0.0015,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Divergent concomitant strabismus","text":"Phenotype: Divergent concomitant strabismus<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0015<br>N cases: 2289<br>N controls: 361237"}
{"pvalue":0.654,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Ectropion of eyelid","text":"Phenotype: Ectropion of eyelid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.654<br>N cases: 1059<br>N controls: 344684"}
{"pvalue":0.691,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Entropion and trichiasis of eyelid","text":"Phenotype: Entropion and trichiasis of eyelid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.691<br>N cases: 2305<br>N controls: 344684"}
{"pvalue":0.719,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Epiphora","text":"Phenotype: Epiphora<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.719<br>N cases: 535<br>N controls: 344684"}
{"pvalue":0.0355,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Episcleritis","text":"Phenotype: Episcleritis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0355<br>N cases: 1392<br>N controls: 357814"}
{"pvalue":0.624,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Exophthalmic conditions","text":"Phenotype: Exophthalmic conditions<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.624<br>N cases: 283<br>N controls: 344684"}
{"pvalue":0.829,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other specified and unspecified disorders of eye and adnexa","text":"Phenotype: Other specified and unspecified disorders of eye and adnexa<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.829<br>N cases: 1074<br>N controls: 373254"}
{"pvalue":0.398,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of eyelid","text":"Phenotype: Other disorders of eyelid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.398<br>N cases: 14347<br>N controls: 344684"}
{"pvalue":0.987,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other disorders affecting eyelid function","text":"Phenotype: Other disorders affecting eyelid function<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.987<br>N cases: 191<br>N controls: 344684"}
{"pvalue":0.279,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other inflammation of eyelid","text":"Phenotype: Other inflammation of eyelid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.279<br>N cases: 3332<br>N controls: 344684"}
{"pvalue":0.228,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Disorders of eyelid in diseases classified elsewhere","text":"Phenotype: Disorders of eyelid in diseases classified elsewhere<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.228<br>N cases: 890<br>N controls: 344684"}
{"pvalue":0.0268,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other specified and unspecified  disorders of eyelid","text":"Phenotype: Other specified and unspecified  disorders of eyelid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0268<br>N cases: 318<br>N controls: 344684"}
{"pvalue":0.975,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of eye and adnexa","text":"Phenotype: Other disorders of eye and adnexa<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.975<br>N cases: 4023<br>N controls: 373254"}
{"pvalue":0.00689,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Primary angle-closure glaucoma","text":"Phenotype: Primary angle-closure glaucoma<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00689<br>N cases: 1199<br>N controls: 358375"}
{"pvalue":0.596,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other and unspecified glaucoma","text":"Phenotype: Other and unspecified glaucoma<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.596<br>N cases: 1638<br>N controls: 358375"}
{"pvalue":0.966,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Glaucoma","text":"Phenotype: Glaucoma<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.966<br>N cases: 18902<br>N controls: 358375"}
{"pvalue":0.377,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Juvenile Open Angle Glaucoma","text":"Phenotype: Juvenile Open Angle Glaucoma<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.377<br>N cases: 151<br>N controls: 377126"}
{"pvalue":0.467,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Use of antiglaucoma preparations and miotics","text":"Phenotype: Use of antiglaucoma preparations and miotics<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.467<br>N cases: 2349<br>N controls: 358375"}
{"pvalue":0.297,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Normotensive glaucoma","text":"Phenotype: Normotensive glaucoma<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.297<br>N cases: 2085<br>N controls: 358375"}
{"pvalue":0.55,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Primary open-angle glaucoma, strict","text":"Phenotype: Primary open-angle glaucoma, strict<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.55<br>N cases: 7756<br>N controls: 358375"}
{"pvalue":0.149,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Glaucoma, exfoliation","text":"Phenotype: Glaucoma, exfoliation<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.149<br>N cases: 3125<br>N controls: 358375"}
{"pvalue":0.661,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Glaucoma secondary to eye inflammation","text":"Phenotype: Glaucoma secondary to eye inflammation<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.661<br>N cases: 211<br>N controls: 358375"}
{"pvalue":0.421,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Glaucoma secondary to eye trauma","text":"Phenotype: Glaucoma secondary to eye trauma<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.421<br>N cases: 166<br>N controls: 358375"}
{"pvalue":0.246,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Glaucoma suspect","text":"Phenotype: Glaucoma suspect<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.246<br>N cases: 10758<br>N controls: 358375"}
{"pvalue":0.81,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Degenerative conditions of globe","text":"Phenotype: Degenerative conditions of globe<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.81<br>N cases: 151<br>N controls: 361552"}
{"pvalue":0.987,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Disorders of globe","text":"Phenotype: Disorders of globe<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.987<br>N cases: 651<br>N controls: 361552"}
{"pvalue":0.263,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Hereditary retinal dystrophy","text":"Phenotype: Hereditary retinal dystrophy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.263<br>N cases: 380<br>N controls: 344569"}
{"pvalue":0.162,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Herpesviral keratitis and keratoconjunctivitis","text":"Phenotype: Herpesviral keratitis and keratoconjunctivitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.162<br>N cases: 1145<br>N controls: 357814"}
{"pvalue":0.863,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Heterophoria","text":"Phenotype: Heterophoria<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.863<br>N cases: 2233<br>N controls: 361237"}
{"pvalue":0.534,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Hordeolum and other deep inflammation of eyelid","text":"Phenotype: Hordeolum and other deep inflammation of eyelid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.534<br>N cases: 1320<br>N controls: 344684"}
{"pvalue":0.578,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Hypermetropia","text":"Phenotype: Hypermetropia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.578<br>N cases: 1734<br>N controls: 361237"}
{"pvalue":0.592,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Intermittent heterotropia","text":"Phenotype: Intermittent heterotropia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.592<br>N cases: 1617<br>N controls: 361237"}
{"pvalue":0.62,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Internuclear ophthalmoplegia","text":"Phenotype: Internuclear ophthalmoplegia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.62<br>N cases: 93<br>N controls: 361237"}
{"pvalue":0.432,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Acute and subacute iridocyclitis","text":"Phenotype: Acute and subacute iridocyclitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.432<br>N cases: 6166<br>N controls: 357814"}
{"pvalue":0.0993,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Chronic iridocyclitis","text":"Phenotype: Chronic iridocyclitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0993<br>N cases: 1401<br>N controls: 357814"}
{"pvalue":0.429,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Anterior Iridocyclitis","text":"Phenotype: Anterior Iridocyclitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.429<br>N cases: 6536<br>N controls: 370741"}
{"pvalue":0.449,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Iridocyclitis","text":"Phenotype: Iridocyclitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.449<br>N cases: 7306<br>N controls: 357814"}
{"pvalue":0.675,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Iridocyclitis in diseases classified elsewhere","text":"Phenotype: Iridocyclitis in diseases classified elsewhere<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.675<br>N cases: 422<br>N controls: 357814"}
{"pvalue":0.31,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other and unspecified iridocyclitis","text":"Phenotype: Other and unspecified iridocyclitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.31<br>N cases: 1069<br>N controls: 357814"}
{"pvalue":0.0571,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other specified and unspecified disorders of iris and ciliary body","text":"Phenotype: Other specified and unspecified disorders of iris and ciliary body<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0571<br>N cases: 99<br>N controls: 357814"}
{"pvalue":0.261,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Keratitis","text":"Phenotype: Keratitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.261<br>N cases: 11611<br>N controls: 357814"}
{"pvalue":0.459,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Keratitis and keratoconjunctivitis in other diseases classified elsewhere","text":"Phenotype: Keratitis and keratoconjunctivitis in other diseases classified elsewhere<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.459<br>N cases: 967<br>N controls: 357814"}
{"pvalue":0.276,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other keratitis","text":"Phenotype: Other keratitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.276<br>N cases: 3169<br>N controls: 357814"}
{"pvalue":0.0436,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Hereditary corneal dystrophies","text":"Phenotype: Hereditary corneal dystrophies<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0436<br>N cases: 725<br>N controls: 357814"}
{"pvalue":0.763,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Disorders of lacrimal system","text":"Phenotype: Disorders of lacrimal system<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.763<br>N cases: 13326<br>N controls: 344684"}
{"pvalue":0.247,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Inflammation of lacrimal passages (acute and unspecified)","text":"Phenotype: Inflammation of lacrimal passages (acute and unspecified)<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.247<br>N cases: 435<br>N controls: 344684"}
{"pvalue":0.147,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Inflammation of lacrimal passages (chronic)","text":"Phenotype: Inflammation of lacrimal passages (chronic)<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.147<br>N cases: 434<br>N controls: 344684"}
{"pvalue":0.453,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Lagophthalmos","text":"Phenotype: Lagophthalmos<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.453<br>N cases: 281<br>N controls: 344684"}
{"pvalue":0.725,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Dislocation of lens","text":"Phenotype: Dislocation of lens<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.725<br>N cases: 417<br>N controls: 312864"}
{"pvalue":0.807,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Disorders of eyelid, lacrimal system and orbit","text":"Phenotype: Disorders of eyelid, lacrimal system and orbit<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.807<br>N cases: 32593<br>N controls: 344684"}
{"pvalue":0.929,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Degeneration of macula and posterior pole","text":"Phenotype: Degeneration of macula and posterior pole<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.929<br>N cases: 15137<br>N controls: 344569"}
{"pvalue":0.89,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Mild or no visual impairment, binocular","text":"Phenotype: Mild or no visual impairment, binocular<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.89<br>N cases: 120<br>N controls: 360091"}
{"pvalue":0.606,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Moderate visual impairment, binocular","text":"Phenotype: Moderate visual impairment, binocular<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.606<br>N cases: 840<br>N controls: 360091"}
{"pvalue":0.773,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Moderate visual impairment, monocular","text":"Phenotype: Moderate visual impairment, monocular<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.773<br>N cases: 98<br>N controls: 360091"}
{"pvalue":0.957,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Myopia","text":"Phenotype: Myopia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.957<br>N cases: 3534<br>N controls: 361237"}
{"pvalue":0.43,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Nystagmus and other irregular eye movements","text":"Phenotype: Nystagmus and other irregular eye movements<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.43<br>N cases: 346<br>N controls: 373254"}
{"pvalue":0.157,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Disorders of ocular muscles, binocular movement, accommodation and refraction","text":"Phenotype: Disorders of ocular muscles, binocular movement, accommodation and refraction<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.157<br>N cases: 16040<br>N controls: 361237"}
{"pvalue":0.621,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Ocular pain","text":"Phenotype: Ocular pain<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.621<br>N cases: 2121<br>N controls: 373254"}
{"pvalue":0.535,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Optic atrophy","text":"Phenotype: Optic atrophy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.535<br>N cases: 430<br>N controls: 374574"}
{"pvalue":0.0655,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of optic disc","text":"Phenotype: Other disorders of optic disc<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0655<br>N cases: 292<br>N controls: 374574"}
{"pvalue":0.181,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Disorders of optic nerve and visual pathways","text":"Phenotype: Disorders of optic nerve and visual pathways<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.181<br>N cases: 2703<br>N controls: 374574"}
{"pvalue":0.0483,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Disorders of optic nerve, not elsewhere classified","text":"Phenotype: Disorders of optic nerve, not elsewhere classified<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0483<br>N cases: 504<br>N controls: 374574"}
{"pvalue":0.735,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Optic neuritis","text":"Phenotype: Optic neuritis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.735<br>N cases: 1202<br>N controls: 374574"}
{"pvalue":0.17,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of optic [2nd] nerve and visual pathways","text":"Phenotype: Other disorders of optic [2nd] nerve and visual pathways<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.17<br>N cases: 1631<br>N controls: 374574"}
{"pvalue":0.27,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Disorders of orbit","text":"Phenotype: Disorders of orbit<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.27<br>N cases: 1199<br>N controls: 344684"}
{"pvalue":0.809,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Acute inflammation of orbit","text":"Phenotype: Acute inflammation of orbit<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.809<br>N cases: 167<br>N controls: 344684"}
{"pvalue":0.252,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other and unspecified disorders of orbit","text":"Phenotype: Other and unspecified disorders of orbit<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.252<br>N cases: 117<br>N controls: 344684"}
{"pvalue":0.314,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other endophthalmitis","text":"Phenotype: Other endophthalmitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.314<br>N cases: 136<br>N controls: 361552"}
{"pvalue":0.661,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of conjunctiva","text":"Phenotype: Other disorders of conjunctiva<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.661<br>N cases: 3927<br>N controls: 345122"}
{"pvalue":0.486,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other disorders of iris and ciliary body","text":"Phenotype: Other disorders of iris and ciliary body<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.486<br>N cases: 670<br>N controls: 357814"}
{"pvalue":0.374,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other retinal artery occlusion","text":"Phenotype: Other retinal artery occlusion<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.374<br>N cases: 569<br>N controls: 344569"}
{"pvalue":0.715,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Papilloedema, unspecified","text":"Phenotype: Papilloedema, unspecified<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.715<br>N cases: 545<br>N controls: 374574"}
{"pvalue":0.043,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Third [oculomotor] nerve palsy","text":"Phenotype: Third [oculomotor] nerve palsy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.043<br>N cases: 460<br>N controls: 361237"}
{"pvalue":0.564,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Fourth [trochlear] nerve palsy","text":"Phenotype: Fourth [trochlear] nerve palsy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.564<br>N cases: 571<br>N controls: 361237"}
{"pvalue":0.622,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Sixth [abducent] nerve palsy","text":"Phenotype: Sixth [abducent] nerve palsy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.622<br>N cases: 810<br>N controls: 361237"}
{"pvalue":0.236,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Paralytic strabismus","text":"Phenotype: Paralytic strabismus<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.236<br>N cases: 1905<br>N controls: 361237"}
{"pvalue":0.553,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other or unspecified paralytic strabismus","text":"Phenotype: Other or unspecified paralytic strabismus<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.553<br>N cases: 177<br>N controls: 361237"}
{"pvalue":0.547,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Peripheral retinal degeneration","text":"Phenotype: Peripheral retinal degeneration<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.547<br>N cases: 810<br>N controls: 344569"}
{"pvalue":0.297,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Presbyopia","text":"Phenotype: Presbyopia<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.297<br>N cases: 1327<br>N controls: 361237"}
{"pvalue":0.506,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other proliferative retinopathy","text":"Phenotype: Other proliferative retinopathy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.506<br>N cases: 122<br>N controls: 344569"}
{"pvalue":0.189,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Pterygium","text":"Phenotype: Pterygium<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.189<br>N cases: 718<br>N controls: 345122"}
{"pvalue":0.278,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Ptosis of eyelid","text":"Phenotype: Ptosis of eyelid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.278<br>N cases: 2807<br>N controls: 344684"}
{"pvalue":0.22,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Purulent endophthalmitis","text":"Phenotype: Purulent endophthalmitis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.22<br>N cases: 140<br>N controls: 361552"}
{"pvalue":0.946,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Disorders of refraction and accommodation","text":"Phenotype: Disorders of refraction and accommodation<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.946<br>N cases: 7737<br>N controls: 361237"}
{"pvalue":0.0704,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Retinal haemorrhage","text":"Phenotype: Retinal haemorrhage<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0704<br>N cases: 569<br>N controls: 344569"}
{"pvalue":0.0686,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Retinal breaks without detachment","text":"Phenotype: Retinal breaks without detachment<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0686<br>N cases: 4390<br>N controls: 344569"}
{"pvalue":0.557,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Retinal detachment with retinal break","text":"Phenotype: Retinal detachment with retinal break<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.557<br>N cases: 3712<br>N controls: 344569"}
{"pvalue":0.154,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Retinal detachments and breaks","text":"Phenotype: Retinal detachments and breaks<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.154<br>N cases: 11230<br>N controls: 344569"}
{"pvalue":0.781,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other, unspecified and serous retinal detachments","text":"Phenotype: Other, unspecified and serous retinal detachments<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.781<br>N cases: 765<br>N controls: 344569"}
{"pvalue":0.402,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Traction detachment of retina","text":"Phenotype: Traction detachment of retina<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.402<br>N cases: 223<br>N controls: 344569"}
{"pvalue":0.438,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other retinal disorders","text":"Phenotype: Other retinal disorders<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.438<br>N cases: 23610<br>N controls: 344569"}
{"pvalue":0.0172,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other specified and unspecified retinal disorders","text":"Phenotype: Other specified and unspecified retinal disorders<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0172<br>N cases: 847<br>N controls: 344569"}
{"pvalue":0.968,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Separation of retinal layers (serosa)","text":"Phenotype: Separation of retinal layers (serosa)<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.968<br>N cases: 1068<br>N controls: 344569"}
{"pvalue":0.421,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Retinal vascular disorders","text":"Phenotype: Retinal vascular disorders<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.421<br>N cases: 3447<br>N controls: 344569"}
{"pvalue":0.337,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Retinoschisis and retinal cysts","text":"Phenotype: Retinoschisis and retinal cysts<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.337<br>N cases: 579<br>N controls: 344569"}
{"pvalue":0.183,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Diabetic background retinopathy","text":"Phenotype: Diabetic background retinopathy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.183<br>N cases: 4011<br>N controls: 344569"}
{"pvalue":0.407,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Severe diabetic background retinopathy","text":"Phenotype: Severe diabetic background retinopathy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.407<br>N cases: 816<br>N controls: 344569"}
{"pvalue":0.225,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Diabetic retinopathy","text":"Phenotype: Diabetic retinopathy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.225<br>N cases: 6818<br>N controls: 344569"}
{"pvalue":0.15,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other diabetic retinopathy","text":"Phenotype: Other diabetic retinopathy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.15<br>N cases: 1912<br>N controls: 344569"}
{"pvalue":0.895,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Proliferative diabetic retinopathy","text":"Phenotype: Proliferative diabetic retinopathy<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.895<br>N cases: 2468<br>N controls: 344569"}
{"pvalue":0.487,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Retinopathy of prematurity","text":"Phenotype: Retinopathy of prematurity<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.487<br>N cases: 87<br>N controls: 344569"}
{"pvalue":0.5,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Retinal vascular occlusion","text":"Phenotype: Retinal vascular occlusion<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.5<br>N cases: 3342<br>N controls: 344569"}
{"pvalue":0.0814,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Retrobulbar neuritis in diseases classified elsewhere","text":"Phenotype: Retrobulbar neuritis in diseases classified elsewhere<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0814<br>N cases: 95<br>N controls: 374574"}
{"pvalue":0.834,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Disorders of sclera, cornea, iris and ciliary body","text":"Phenotype: Disorders of sclera, cornea, iris and ciliary body<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.834<br>N cases: 19463<br>N controls: 357814"}
{"pvalue":0.607,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Scleritis","text":"Phenotype: Scleritis<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.607<br>N cases: 290<br>N controls: 357814"}
{"pvalue":0.675,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Severe visual impairment, binocular","text":"Phenotype: Severe visual impairment, binocular<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.675<br>N cases: 122<br>N controls: 360091"}
{"pvalue":0.221,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Severe visual impairment, monocular","text":"Phenotype: Severe visual impairment, monocular<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.221<br>N cases: 180<br>N controls: 360091"}
{"pvalue":0.795,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Stenosis and insufficiency of lacrimal passages","text":"Phenotype: Stenosis and insufficiency of lacrimal passages<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.795<br>N cases: 2653<br>N controls: 344684"}
{"pvalue":0.0329,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Other specified and unspecified strabismus","text":"Phenotype: Other specified and unspecified strabismus<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0329<br>N cases: 275<br>N controls: 361237"}
{"pvalue":0.105,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other strabismus","text":"Phenotype: Other strabismus<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.105<br>N cases: 7179<br>N controls: 361237"}
{"pvalue":0.883,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Hyphaema and other vascular disorders of iris and ciliary body","text":"Phenotype: Hyphaema and other vascular disorders of iris and ciliary body<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.883<br>N cases: 467<br>N controls: 357814"}
{"pvalue":0.908,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Vertical strabismus","text":"Phenotype: Vertical strabismus<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.908<br>N cases: 873<br>N controls: 361237"}
{"pvalue":0.213,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other and unspecified visual disturbances","text":"Phenotype: Other and unspecified visual disturbances<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.213<br>N cases: 2382<br>N controls: 360091"}
{"pvalue":0.688,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Visual field defects","text":"Phenotype: Visual field defects<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.688<br>N cases: 2373<br>N controls: 360091"}
{"pvalue":0.456,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Blindness or visual impairment, binocular","text":"Phenotype: Blindness or visual impairment, binocular<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.456<br>N cases: 117<br>N controls: 360091"}
{"pvalue":0.148,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Visual disturbances","text":"Phenotype: Visual disturbances<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.148<br>N cases: 15707<br>N controls: 360091"}
{"pvalue":0.602,"sign":1,"group":"H7: Eye and adnexa diseases","label":"Subjective visual disturbances","text":"Phenotype: Subjective visual disturbances<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.602<br>N cases: 7313<br>N controls: 360091"}
{"pvalue":0.538,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Disorders of vitreous body","text":"Phenotype: Disorders of vitreous body<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.538<br>N cases: 15177<br>N controls: 361552"}
{"pvalue":0.278,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Crystalline deposits in vitreous body","text":"Phenotype: Crystalline deposits in vitreous body<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.278<br>N cases: 202<br>N controls: 361552"}
{"pvalue":0.122,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other vitreous opacities","text":"Phenotype: Other vitreous opacities<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.122<br>N cases: 993<br>N controls: 361552"}
{"pvalue":0.797,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Other and unspecified disorders of vitreous body","text":"Phenotype: Other and unspecified disorders of vitreous body<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.797<br>N cases: 12004<br>N controls: 361552"}
{"pvalue":0.286,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Xanthelasma of eyelid","text":"Phenotype: Xanthelasma of eyelid<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.286<br>N cases: 228<br>N controls: 344684"}
{"pvalue":0.229,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Other abnormal auditory perceptions","text":"Phenotype: Other abnormal auditory perceptions<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.229<br>N cases: 261<br>N controls: 331736"}
{"pvalue":0.415,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Benign paroxysmal vertigo","text":"Phenotype: Benign paroxysmal vertigo<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.415<br>N cases: 8280<br>N controls: 359094"}
{"pvalue":0.519,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Impacted cerumen","text":"Phenotype: Impacted cerumen<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.519<br>N cases: 2253<br>N controls: 367005"}
{"pvalue":0.404,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Cholesteatoma of middle ear","text":"Phenotype: Cholesteatoma of middle ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.404<br>N cases: 1447<br>N controls: 352571"}
{"pvalue":0.356,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Chronic suppurative otitis media","text":"Phenotype: Chronic suppurative otitis media<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.356<br>N cases: 2101<br>N controls: 352571"}
{"pvalue":0.961,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Discontinuity and dislocation of ear ossicles","text":"Phenotype: Discontinuity and dislocation of ear ossicles<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.961<br>N cases: 126<br>N controls: 352571"}
{"pvalue":0.674,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Other disorders of Eustachian tube","text":"Phenotype: Other disorders of Eustachian tube<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.674<br>N cases: 686<br>N controls: 352571"}
{"pvalue":0.312,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Eustachian salpingitis and obstruction","text":"Phenotype: Eustachian salpingitis and obstruction<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.312<br>N cases: 2425<br>N controls: 352571"}
{"pvalue":0.716,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Abscess of external ear","text":"Phenotype: Abscess of external ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.716<br>N cases: 375<br>N controls: 367005"}
{"pvalue":0.89,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Cellulitis of external ear","text":"Phenotype: Cellulitis of external ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.89<br>N cases: 307<br>N controls: 367005"}
{"pvalue":0.789,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Cholesteatoma of external ear","text":"Phenotype: Cholesteatoma of external ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.789<br>N cases: 157<br>N controls: 367005"}
{"pvalue":0.195,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Disorder of external ear, unspecified","text":"Phenotype: Disorder of external ear, unspecified<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.195<br>N cases: 770<br>N controls: 367005"}
{"pvalue":0.39,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Other specified disorders of external ear","text":"Phenotype: Other specified disorders of external ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.39<br>N cases: 923<br>N controls: 367005"}
{"pvalue":0.113,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Diseases of external ear","text":"Phenotype: Diseases of external ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.113<br>N cases: 10272<br>N controls: 367005"}
{"pvalue":0.546,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Other infective otitis externa","text":"Phenotype: Other infective otitis externa<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.546<br>N cases: 1621<br>N controls: 367005"}
{"pvalue":0.2,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Otitis externa, unspecified","text":"Phenotype: Otitis externa, unspecified<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.2<br>N cases: 2934<br>N controls: 367005"}
{"pvalue":0.298,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Acute otitis externa, noninfective","text":"Phenotype: Acute otitis externa, noninfective<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.298<br>N cases: 435<br>N controls: 367005"}
{"pvalue":0.706,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Other otitis externa (chronic)","text":"Phenotype: Other otitis externa (chronic)<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.706<br>N cases: 1700<br>N controls: 367005"}
{"pvalue":0.0274,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Otitis externa","text":"Phenotype: Otitis externa<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0274<br>N cases: 6547<br>N controls: 367005"}
{"pvalue":0.569,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Conductive hearing loss, unspecified","text":"Phenotype: Conductive hearing loss, unspecified<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.569<br>N cases: 2398<br>N controls: 331736"}
{"pvalue":0.183,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Deaf mutism, not elsewhere classified","text":"Phenotype: Deaf mutism, not elsewhere classified<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.183<br>N cases: 147<br>N controls: 331736"}
{"pvalue":0.289,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Sudden idiopathic hearing loss","text":"Phenotype: Sudden idiopathic hearing loss<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.289<br>N cases: 2848<br>N controls: 331736"}
{"pvalue":0.101,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Mixed conductive and sensorineural hearing loss","text":"Phenotype: Mixed conductive and sensorineural hearing loss<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.101<br>N cases: 3581<br>N controls: 331736"}
{"pvalue":0.604,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Other specified/unspecified hearing loss","text":"Phenotype: Other specified/unspecified hearing loss<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.604<br>N cases: 2105<br>N controls: 331736"}
{"pvalue":0.915,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Presbycusis","text":"Phenotype: Presbycusis<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.915<br>N cases: 4140<br>N controls: 331736"}
{"pvalue":0.0482,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Sensorineural hearing loss","text":"Phenotype: Sensorineural hearing loss<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0482<br>N cases: 32487<br>N controls: 331736"}
{"pvalue":0.789,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Other specified/unspecified diseases of inner ear","text":"Phenotype: Other specified/unspecified diseases of inner ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.789<br>N cases: 123<br>N controls: 359094"}
{"pvalue":0.659,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Labyrinthine fistula","text":"Phenotype: Labyrinthine fistula<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.659<br>N cases: 80<br>N controls: 359094"}
{"pvalue":0.373,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Labyrinthitis","text":"Phenotype: Labyrinthitis<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.373<br>N cases: 80<br>N controls: 359094"}
{"pvalue":0.25,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Acute mastoiditis","text":"Phenotype: Acute mastoiditis<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.25<br>N cases: 246<br>N controls: 352571"}
{"pvalue":0.804,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Chronic mastoiditis","text":"Phenotype: Chronic mastoiditis<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.804<br>N cases: 727<br>N controls: 352571"}
{"pvalue":0.0115,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Other/unspecified mastoiditis and related conditions","text":"Phenotype: Other/unspecified mastoiditis and related conditions<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0115<br>N cases: 122<br>N controls: 352571"}
{"pvalue":0.043,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Suppurative and unspecified otitis media","text":"Phenotype: Suppurative and unspecified otitis media<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.043<br>N cases: 14406<br>N controls: 352571"}
{"pvalue":0.636,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Ménière disease","text":"Phenotype: Ménière disease<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.636<br>N cases: 2746<br>N controls: 359094"}
{"pvalue":0.209,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Adhesive middle ear disease","text":"Phenotype: Adhesive middle ear disease<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.209<br>N cases: 444<br>N controls: 352571"}
{"pvalue":0.0442,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Diseases of middle ear and mastoid","text":"Phenotype: Diseases of middle ear and mastoid<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0442<br>N cases: 24706<br>N controls: 352571"}
{"pvalue":0.763,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Acute myringitis","text":"Phenotype: Acute myringitis<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.763<br>N cases: 167<br>N controls: 352571"}
{"pvalue":0.976,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Chronic myringitis","text":"Phenotype: Chronic myringitis<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.976<br>N cases: 106<br>N controls: 352571"}
{"pvalue":0.826,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Noise effects on inner ear","text":"Phenotype: Noise effects on inner ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.826<br>N cases: 1050<br>N controls: 359094"}
{"pvalue":0.0797,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Nonsuppurative otitis media","text":"Phenotype: Nonsuppurative otitis media<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0797<br>N cases: 8315<br>N controls: 352571"}
{"pvalue":0.248,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Otalgia","text":"Phenotype: Otalgia<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.248<br>N cases: 2004<br>N controls: 331736"}
{"pvalue":0.11,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Other disorders of ear","text":"Phenotype: Other disorders of ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.11<br>N cases: 45541<br>N controls: 331736"}
{"pvalue":0.898,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Other hearing loss","text":"Phenotype: Other hearing loss<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.898<br>N cases: 8833<br>N controls: 331736"}
{"pvalue":0.241,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Otitis media, unspecified","text":"Phenotype: Otitis media, unspecified<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.241<br>N cases: 3511<br>N controls: 352571"}
{"pvalue":0.604,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Otorrhagia","text":"Phenotype: Otorrhagia<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.604<br>N cases: 152<br>N controls: 331736"}
{"pvalue":0.511,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Otosclerosis","text":"Phenotype: Otosclerosis<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.511<br>N cases: 2269<br>N controls: 359094"}
{"pvalue":0.172,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Perichondritis of external ear","text":"Phenotype: Perichondritis of external ear<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.172<br>N cases: 431<br>N controls: 367005"}
{"pvalue":0.863,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Perforation of tympanic membrane","text":"Phenotype: Perforation of tympanic membrane<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.863<br>N cases: 2814<br>N controls: 352571"}
{"pvalue":0.29,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Other peripheral vertigo","text":"Phenotype: Other peripheral vertigo<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.29<br>N cases: 2523<br>N controls: 359094"}
{"pvalue":0.883,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Recurrent cholesteatoma of postmastoidectomy cavity","text":"Phenotype: Recurrent cholesteatoma of postmastoidectomy cavity<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.883<br>N cases: 87<br>N controls: 331736"}
{"pvalue":0.491,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Other disorders following mastoidectomy","text":"Phenotype: Other disorders following mastoidectomy<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.491<br>N cases: 89<br>N controls: 331736"}
{"pvalue":0.773,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Postprocedural disorders of ear and mastoid process, not elsewhere classified","text":"Phenotype: Postprocedural disorders of ear and mastoid process, not elsewhere classified<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.773<br>N cases: 206<br>N controls: 331736"}
{"pvalue":0.513,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Acquired stenosis of external ear canal","text":"Phenotype: Acquired stenosis of external ear canal<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.513<br>N cases: 217<br>N controls: 367005"}
{"pvalue":0.0126,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Acute suppurative otitis media","text":"Phenotype: Acute suppurative otitis media<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0126<br>N cases: 9850<br>N controls: 352571"}
{"pvalue":0.035,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Suppurative otitis media, unspecified","text":"Phenotype: Suppurative otitis media, unspecified<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.035<br>N cases: 722<br>N controls: 352571"}
{"pvalue":0.858,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Tinnitus","text":"Phenotype: Tinnitus<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.858<br>N cases: 7175<br>N controls: 331736"}
{"pvalue":0.168,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Vertigo of central origin","text":"Phenotype: Vertigo of central origin<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.168<br>N cases: 388<br>N controls: 359094"}
{"pvalue":0.739,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Disorders of vestibular function (Vertigo)","text":"Phenotype: Disorders of vestibular function (Vertigo)<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.739<br>N cases: 14918<br>N controls: 359094"}
{"pvalue":0.306,"sign":-1,"group":"H8: Ear and mastoid process diseases","label":"Vestibular neuronitis","text":"Phenotype: Vestibular neuronitis<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.306<br>N cases: 2379<br>N controls: 359094"}
{"pvalue":0.589,"sign":1,"group":"H8: Ear and mastoid process diseases","label":"Other/unspecified disorders of vestibular function","text":"Phenotype: Other/unspecified disorders of vestibular function<br>Category: H8: Ear and mastoid process diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.589<br>N cases: 891<br>N controls: 359094"}
{"pvalue":0.404,"sign":-1,"group":"K11: Digestive system diseases","label":"Inguinal hernia, bilateral","text":"Phenotype: Inguinal hernia, bilateral<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.404<br>N cases: 2998<br>N controls: 322586"}
{"pvalue":0.707,"sign":1,"group":"K11: Digestive system diseases","label":"Inguinal hernia, unilateral","text":"Phenotype: Inguinal hernia, unilateral<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.707<br>N cases: 705<br>N controls: 322586"}
{"pvalue":0.122,"sign":1,"group":"I9: Circulatory system diseases","label":"Hypotension due to drugs","text":"Phenotype: Hypotension due to drugs<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.122<br>N cases: 342<br>N controls: 376935"}
{"pvalue":0.673,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Hypothyroidism, drug reimbursement","text":"Phenotype: Hypothyroidism, drug reimbursement<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.673<br>N cases: 12040<br>N controls: 88531"}
{"pvalue":7.64e-08,"sign":-1,"group":"I9: Circulatory system diseases","label":"Abdominal aortic aneurysm (AAA)","text":"Phenotype: Abdominal aortic aneurysm (AAA)<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 7.64e-08<br>N cases: 3548<br>N controls: 349539"}
{"pvalue":0.00147,"sign":-1,"group":"I9: Circulatory system diseases","label":"Atrial fibrillation and flutter","text":"Phenotype: Atrial fibrillation and flutter<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00147<br>N cases: 45766<br>N controls: 191924"}
{"pvalue":0.0213,"sign":-1,"group":"I9: Circulatory system diseases","label":"Atrial fibrillation and flutter with reimbursement","text":"Phenotype: Atrial fibrillation and flutter with reimbursement<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0213<br>N cases: 21700<br>N controls: 191924"}
{"pvalue":0.922,"sign":1,"group":"I9: Circulatory system diseases","label":"Cerebral aneurysm, nonruptured","text":"Phenotype: Cerebral aneurysm, nonruptured<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.922<br>N cases: 2582<br>N controls: 342673"}
{"pvalue":0.00019,"sign":-1,"group":"I9: Circulatory system diseases","label":"Angina pectoris","text":"Phenotype: Angina pectoris<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.000191<br>N cases: 34456<br>N controls: 313400"}
{"pvalue":0.00001,"sign":-1,"group":"I9: Circulatory system diseases","label":"Coronary angioplasty","text":"Phenotype: Coronary angioplasty<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 1.24e-05<br>N cases: 14723<br>N controls: 313400"}
{"pvalue":4e-06,"sign":-1,"group":"I9: Circulatory system diseases","label":"Aortic aneurysm","text":"Phenotype: Aortic aneurysm<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 4e-06<br>N cases: 7395<br>N controls: 349539"}
{"pvalue":0.493,"sign":-1,"group":"I9: Circulatory system diseases","label":"Dissection of aorta","text":"Phenotype: Dissection of aorta<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.493<br>N cases: 881<br>N controls: 349539"}
{"pvalue":0.868,"sign":-1,"group":"I9: Circulatory system diseases","label":"Arterial embolism and thrombosis","text":"Phenotype: Arterial embolism and thrombosis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.868<br>N cases: 1735<br>N controls: 349539"}
{"pvalue":0.712,"sign":1,"group":"I9: Circulatory system diseases","label":"Arterial embolism and thrombosis of lower extremity artery","text":"Phenotype: Arterial embolism and thrombosis of lower extremity artery<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.712<br>N cases: 985<br>N controls: 349539"}
{"pvalue":0.754,"sign":-1,"group":"I9: Circulatory system diseases","label":"Other arterial embolism and thrombosis","text":"Phenotype: Other arterial embolism and thrombosis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.754<br>N cases: 812<br>N controls: 349539"}
{"pvalue":0.671,"sign":1,"group":"I9: Circulatory system diseases","label":"Other diseases of arteries and capillaries","text":"Phenotype: Other diseases of arteries and capillaries<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.671<br>N cases: 2679<br>N controls: 349539"}
{"pvalue":0.00006,"sign":-1,"group":"I9: Circulatory system diseases","label":"Atherosclerosis, excluding cerebral, coronary and PAD","text":"Phenotype: Atherosclerosis, excluding cerebral, coronary and PAD<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 5.56e-05<br>N cases: 15002<br>N controls: 349539"}
{"pvalue":0.753,"sign":1,"group":"I9: Circulatory system diseases","label":"AV-block","text":"Phenotype: AV-block<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.753<br>N cases: 5536<br>N controls: 286109"}
{"pvalue":0.00001,"sign":-1,"group":"I9: Circulatory system diseases","label":"Coronary artery bypass grafting","text":"Phenotype: Coronary artery bypass grafting<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 1.49e-05<br>N cases: 10938<br>N controls: 313400"}
{"pvalue":0.18,"sign":-1,"group":"I9: Circulatory system diseases","label":"Cardiac arrest","text":"Phenotype: Cardiac arrest<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.18<br>N cases: 2308<br>N controls: 191924"}
{"pvalue":0.832,"sign":1,"group":"I9: Circulatory system diseases","label":"Cardiomyopathies, Secondary/extrinsic","text":"Phenotype: Cardiomyopathies, Secondary/extrinsic<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.832<br>N cases: 156<br>N controls: 286109"}
{"pvalue":0.892,"sign":1,"group":"I9: Circulatory system diseases","label":"Alcoholic cardiomyopathy","text":"Phenotype: Alcoholic cardiomyopathy<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.892<br>N cases: 124<br>N controls: 371403"}
{"pvalue":0.621,"sign":-1,"group":"I9: Circulatory system diseases","label":"Cardiomyopathy","text":"Phenotype: Cardiomyopathy<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.621<br>N cases: 5874<br>N controls: 286109"}
{"pvalue":0.555,"sign":-1,"group":"I9: Circulatory system diseases","label":"Cardiomyopathy, Hypertrophic obstructive","text":"Phenotype: Cardiomyopathy, Hypertrophic obstructive<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.555<br>N cases: 519<br>N controls: 286109"}
{"pvalue":0.679,"sign":1,"group":"I9: Circulatory system diseases","label":"Cardiomyopathy in other diseases","text":"Phenotype: Cardiomyopathy in other diseases<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.679<br>N cases: 124<br>N controls: 286109"}
{"pvalue":0.895,"sign":-1,"group":"I9: Circulatory system diseases","label":"Cardiomyopathy, other and unspecified","text":"Phenotype: Cardiomyopathy, other and unspecified<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.895<br>N cases: 2412<br>N controls: 286109"}
{"pvalue":0.443,"sign":-1,"group":"I9: Circulatory system diseases","label":"Restrictive cardiomyopathy","text":"Phenotype: Restrictive cardiomyopathy<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.443<br>N cases: 96<br>N controls: 371403"}
{"pvalue":0.0653,"sign":-1,"group":"I9: Circulatory system diseases","label":"Calcific aortic valvular stenosis, operated","text":"Phenotype: Calcific aortic valvular stenosis, operated<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0653<br>N cases: 9153<br>N controls: 368124"}
{"pvalue":0.135,"sign":-1,"group":"I9: Circulatory system diseases","label":"Cerebral atherosclerosis","text":"Phenotype: Cerebral atherosclerosis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.135<br>N cases: 322<br>N controls: 376955"}
{"pvalue":0.832,"sign":1,"group":"I9: Circulatory system diseases","label":"Other specified cerebrovascular diseases, other cerebrovascular disorders in diseases classified elsewhere","text":"Phenotype: Other specified cerebrovascular diseases, other cerebrovascular disorders in diseases classified elsewhere<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.832<br>N cases: 1949<br>N controls: 342673"}
{"pvalue":0.00003,"sign":-1,"group":"I9: Circulatory system diseases","label":"Major coronary heart disease event","text":"Phenotype: Major coronary heart disease event<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 2.86e-05<br>N cases: 43518<br>N controls: 333759"}
{"pvalue":0.412,"sign":-1,"group":"I9: Circulatory system diseases","label":"Conduction disorders","text":"Phenotype: Conduction disorders<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.412<br>N cases: 9949<br>N controls: 286109"}
{"pvalue":0.00003,"sign":-1,"group":"I9: Circulatory system diseases","label":"Coronary atherosclerosis","text":"Phenotype: Coronary atherosclerosis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 3.46e-05<br>N cases: 47550<br>N controls: 313400"}
{"pvalue":0.118,"sign":1,"group":"I9: Circulatory system diseases","label":"Dissection of cerebral arteries, nonruptured","text":"Phenotype: Dissection of cerebral arteries, nonruptured<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.118<br>N cases: 180<br>N controls: 342673"}
{"pvalue":0.239,"sign":1,"group":"I9: Circulatory system diseases","label":"Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified","text":"Phenotype: Diseases of veins, lymphatic vessels and lymph nodes, not elsewhere classified<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.239<br>N cases: 53156<br>N controls: 324121"}
{"pvalue":0.0949,"sign":-1,"group":"I9: Circulatory system diseases","label":"Dronedarone medication","text":"Phenotype: Dronedarone medication<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0949<br>N cases: 743<br>N controls: 286109"}
{"pvalue":0.574,"sign":1,"group":"I9: Circulatory system diseases","label":"Endocarditis","text":"Phenotype: Endocarditis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.574<br>N cases: 940<br>N controls: 286109"}
{"pvalue":0.501,"sign":-1,"group":"I9: Circulatory system diseases","label":"All-cause Heart Failure","text":"Phenotype: All-cause Heart Failure<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.501<br>N cases: 26872<br>N controls: 349361"}
{"pvalue":0.439,"sign":-1,"group":"I9: Circulatory system diseases","label":"Heart failure,strict (more control exclusions)","text":"Phenotype: Heart failure,strict (more control exclusions)<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.439<br>N cases: 27304<br>N controls: 328105"}
{"pvalue":0.438,"sign":-1,"group":"I9: Circulatory system diseases","label":"Heart failure,strict","text":"Phenotype: Heart failure,strict<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.438<br>N cases: 27304<br>N controls: 349973"}
{"pvalue":0.529,"sign":-1,"group":"I9: Circulatory system diseases","label":"Hypertensive encephalopathy","text":"Phenotype: Hypertensive encephalopathy<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.529<br>N cases: 96<br>N controls: 342673"}
{"pvalue":0.266,"sign":-1,"group":"I9: Circulatory system diseases","label":"Hypertrophic cardiomyopathy","text":"Phenotype: Hypertrophic cardiomyopathy<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.266<br>N cases: 1044<br>N controls: 376233"}
{"pvalue":0.203,"sign":1,"group":"I9: Circulatory system diseases","label":"Hypotension","text":"Phenotype: Hypotension<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.203<br>N cases: 4432<br>N controls: 371886"}
{"pvalue":0.18,"sign":1,"group":"I9: Circulatory system diseases","label":"Secondary hypertension","text":"Phenotype: Secondary hypertension<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.18<br>N cases: 2597<br>N controls: 191924"}
{"pvalue":0.783,"sign":1,"group":"I9: Circulatory system diseases","label":"Hypertension, essential","text":"Phenotype: Hypertension, essential<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.783<br>N cases: 92462<br>N controls: 265626"}
{"pvalue":0.943,"sign":1,"group":"I9: Circulatory system diseases","label":"Hypertension","text":"Phenotype: Hypertension<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.943<br>N cases: 111581<br>N controls: 265626"}
{"pvalue":0.597,"sign":1,"group":"I9: Circulatory system diseases","label":"Hypertensive Heart Disease","text":"Phenotype: Hypertensive Heart Disease<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.597<br>N cases: 8387<br>N controls: 265626"}
{"pvalue":0.0973,"sign":1,"group":"I9: Circulatory system diseases","label":"Hypertension, Pulmonary Arterial","text":"Phenotype: Hypertension, Pulmonary Arterial<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0973<br>N cases: 234<br>N controls: 265626"}
{"pvalue":0.44,"sign":-1,"group":"I9: Circulatory system diseases","label":"Hypertensive Renal Disease","text":"Phenotype: Hypertensive Renal Disease<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.44<br>N cases: 1022<br>N controls: 265626"}
{"pvalue":0.83,"sign":-1,"group":"I9: Circulatory system diseases","label":"Intracerebral haemmorrhage","text":"Phenotype: Intracerebral haemmorrhage<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.83<br>N cases: 3749<br>N controls: 339914"}
{"pvalue":0.00001,"sign":-1,"group":"I9: Circulatory system diseases","label":"Ischaemic heart disease, wide definition","text":"Phenotype: Ischaemic heart disease, wide definition<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 1.4e-05<br>N cases: 63744<br>N controls: 313533"}
{"pvalue":0.546,"sign":1,"group":"I9: Circulatory system diseases","label":"Nontraumatic intracranial haemmorrhage","text":"Phenotype: Nontraumatic intracranial haemmorrhage<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.546<br>N cases: 6530<br>N controls: 342673"}
{"pvalue":0.00467,"sign":-1,"group":"I9: Circulatory system diseases","label":"Death due to cardiac causes","text":"Phenotype: Death due to cardiac causes<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00467<br>N cases: 19295<br>N controls: 357982"}
{"pvalue":0.223,"sign":-1,"group":"I9: Circulatory system diseases","label":"Left bundle-branch block","text":"Phenotype: Left bundle-branch block<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.223<br>N cases: 1918<br>N controls: 286109"}
{"pvalue":0.316,"sign":1,"group":"I9: Circulatory system diseases","label":"Nonspecific lymphadenitis","text":"Phenotype: Nonspecific lymphadenitis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.316<br>N cases: 1808<br>N controls: 324121"}
{"pvalue":0.75,"sign":-1,"group":"I9: Circulatory system diseases","label":"Other noninfective disorders of lymphatic vessels and lymph nodes","text":"Phenotype: Other noninfective disorders of lymphatic vessels and lymph nodes<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.75<br>N cases: 901<br>N controls: 324121"}
{"pvalue":0.0334,"sign":1,"group":"I9: Circulatory system diseases","label":"Complications following myocardial infarction","text":"Phenotype: Complications following myocardial infarction<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0334<br>N cases: 226<br>N controls: 313400"}
{"pvalue":0.00158,"sign":-1,"group":"I9: Circulatory system diseases","label":"Myocardial infarction, strict","text":"Phenotype: Myocardial infarction, strict<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00158<br>N cases: 24185<br>N controls: 313400"}
{"pvalue":0.22,"sign":1,"group":"I9: Circulatory system diseases","label":"Myocarditis","text":"Phenotype: Myocarditis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.22<br>N cases: 1521<br>N controls: 191924"}
{"pvalue":0.488,"sign":-1,"group":"I9: Circulatory system diseases","label":"Non-ischemic cardiomyopathy","text":"Phenotype: Non-ischemic cardiomyopathy<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.488<br>N cases: 9926<br>N controls: 303607"}
{"pvalue":0.807,"sign":1,"group":"I9: Circulatory system diseases","label":"Nonischemic cardiomyopathy","text":"Phenotype: Nonischemic cardiomyopathy<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.807<br>N cases: 1639<br>N controls: 311340"}
{"pvalue":0.256,"sign":-1,"group":"I9: Circulatory system diseases","label":"Non-rheumatic valve diseases","text":"Phenotype: Non-rheumatic valve diseases<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.256<br>N cases: 20772<br>N controls: 286109"}
{"pvalue":0.649,"sign":-1,"group":"I9: Circulatory system diseases","label":"Other aneurysm","text":"Phenotype: Other aneurysm<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.649<br>N cases: 1530<br>N controls: 349539"}
{"pvalue":0.677,"sign":1,"group":"I9: Circulatory system diseases","label":"Other arrhythmias","text":"Phenotype: Other arrhythmias<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.677<br>N cases: 28079<br>N controls: 286109"}
{"pvalue":0.479,"sign":-1,"group":"I9: Circulatory system diseases","label":"Other or ill-defined heart diseases","text":"Phenotype: Other or ill-defined heart diseases<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.479<br>N cases: 1524<br>N controls: 286109"}
{"pvalue":0.514,"sign":-1,"group":"I9: Circulatory system diseases","label":"Other intracranial haemorrhages","text":"Phenotype: Other intracranial haemorrhages<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.514<br>N cases: 768<br>N controls: 342673"}
{"pvalue":0.179,"sign":-1,"group":"I9: Circulatory system diseases","label":"Other other unspecified disorders of the circulatory system","text":"Phenotype: Other other unspecified disorders of the circulatory system<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.179<br>N cases: 1002<br>N controls: 371886"}
{"pvalue":0.685,"sign":1,"group":"I9: Circulatory system diseases","label":"Other peripheral vascular diseases","text":"Phenotype: Other peripheral vascular diseases<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.685<br>N cases: 2230<br>N controls: 349539"}
{"pvalue":0.177,"sign":1,"group":"I9: Circulatory system diseases","label":"Paroxysmal tachycardia","text":"Phenotype: Paroxysmal tachycardia<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.177<br>N cases: 9604<br>N controls: 191924"}
{"pvalue":0.114,"sign":1,"group":"I9: Circulatory system diseases","label":"Other diseases of pericardium","text":"Phenotype: Other diseases of pericardium<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.114<br>N cases: 1135<br>N controls: 286109"}
{"pvalue":0.0395,"sign":1,"group":"I9: Circulatory system diseases","label":"Pericarditis","text":"Phenotype: Pericarditis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0395<br>N cases: 979<br>N controls: 286109"}
{"pvalue":0.886,"sign":1,"group":"I9: Circulatory system diseases","label":"DVT of lower extremities","text":"Phenotype: DVT of lower extremities<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.886<br>N cases: 9109<br>N controls: 324121"}
{"pvalue":0.00046,"sign":1,"group":"I9: Circulatory system diseases","label":"Phlebitis and thrombophlebitis (not including DVT)","text":"Phenotype: Phlebitis and thrombophlebitis (not including DVT)<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.000465<br>N cases: 7037<br>N controls: 324121"}
{"pvalue":0.00719,"sign":-1,"group":"I9: Circulatory system diseases","label":"Status post-ami","text":"Phenotype: Status post-ami<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00719<br>N cases: 3030<br>N controls: 313400"}
{"pvalue":0.0938,"sign":1,"group":"I9: Circulatory system diseases","label":"Progressive vascular leukoencephalopathy","text":"Phenotype: Progressive vascular leukoencephalopathy<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0938<br>N cases: 673<br>N controls: 342673"}
{"pvalue":0.961,"sign":-1,"group":"I9: Circulatory system diseases","label":"Pulmonary embolism","text":"Phenotype: Pulmonary embolism<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.961<br>N cases: 9243<br>N controls: 367108"}
{"pvalue":0.197,"sign":1,"group":"I9: Circulatory system diseases","label":"Portal vein thrombosis","text":"Phenotype: Portal vein thrombosis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.197<br>N cases: 360<br>N controls: 324121"}
{"pvalue":0.557,"sign":-1,"group":"I9: Circulatory system diseases","label":"Right bundle-branch block","text":"Phenotype: Right bundle-branch block<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.557<br>N cases: 954<br>N controls: 286109"}
{"pvalue":2.87e-07,"sign":-1,"group":"I9: Circulatory system diseases","label":"Coronary revascularization (ANGIO or CABG)","text":"Phenotype: Coronary revascularization (ANGIO or CABG)<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 2.87e-07<br>N cases: 23139<br>N controls: 313400"}
{"pvalue":0.0686,"sign":1,"group":"I9: Circulatory system diseases","label":"Rheumatic fever incl heart disease","text":"Phenotype: Rheumatic fever incl heart disease<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0686<br>N cases: 976<br>N controls: 376301"}
{"pvalue":0.578,"sign":1,"group":"I9: Circulatory system diseases","label":"Rheumatic fever with heart involvement","text":"Phenotype: Rheumatic fever with heart involvement<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.578<br>N cases: 138<br>N controls: 376301"}
{"pvalue":0.174,"sign":1,"group":"I9: Circulatory system diseases","label":"Rheumatic fever without mention of heart involvement","text":"Phenotype: Rheumatic fever without mention of heart involvement<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.174<br>N cases: 97<br>N controls: 377180"}
{"pvalue":0.0148,"sign":1,"group":"I9: Circulatory system diseases","label":"Rheumatic valve diseases","text":"Phenotype: Rheumatic valve diseases<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0148<br>N cases: 703<br>N controls: 376301"}
{"pvalue":0.83,"sign":1,"group":"I9: Circulatory system diseases","label":"Aneurysms, operations, SAH","text":"Phenotype: Aneurysms, operations, SAH<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.83<br>N cases: 5342<br>N controls: 342673"}
{"pvalue":0.444,"sign":1,"group":"I9: Circulatory system diseases","label":"Subarachnoid haemmorrhage","text":"Phenotype: Subarachnoid haemmorrhage<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.444<br>N cases: 3289<br>N controls: 339922"}
{"pvalue":0.791,"sign":1,"group":"I9: Circulatory system diseases","label":"Secondary right heart disease","text":"Phenotype: Secondary right heart disease<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.791<br>N cases: 1068<br>N controls: 367108"}
{"pvalue":0.643,"sign":-1,"group":"I9: Circulatory system diseases","label":"Sequelae of cerebrovascular disease","text":"Phenotype: Sequelae of cerebrovascular disease<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.643<br>N cases: 11408<br>N controls: 342673"}
{"pvalue":0.27,"sign":-1,"group":"I9: Circulatory system diseases","label":"Occlusion and stenosis of arteries, not leading to stroke","text":"Phenotype: Occlusion and stenosis of arteries, not leading to stroke<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.27<br>N cases: 406<br>N controls: 342673"}
{"pvalue":0.123,"sign":-1,"group":"I9: Circulatory system diseases","label":"Embolic stroke","text":"Phenotype: Embolic stroke<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.123<br>N cases: 1373<br>N controls: 342673"}
{"pvalue":0.0115,"sign":-1,"group":"I9: Circulatory system diseases","label":"Embolic stroke with flimmer","text":"Phenotype: Embolic stroke with flimmer<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0115<br>N cases: 679<br>N controls: 331511"}
{"pvalue":0.119,"sign":-1,"group":"I9: Circulatory system diseases","label":"Stroke, excluding SAH","text":"Phenotype: Stroke, excluding SAH<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.119<br>N cases: 25398<br>N controls: 339920"}
{"pvalue":0.0244,"sign":-1,"group":"I9: Circulatory system diseases","label":"Thoracic aortic aneurysm","text":"Phenotype: Thoracic aortic aneurysm<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0244<br>N cases: 3510<br>N controls: 349539"}
{"pvalue":0.0947,"sign":1,"group":"I9: Circulatory system diseases","label":"Thromboangiitis obliterans","text":"Phenotype: Thromboangiitis obliterans<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0947<br>N cases: 108<br>N controls: 349539"}
{"pvalue":0.909,"sign":1,"group":"I9: Circulatory system diseases","label":"Nonpyogenic thrombosis of intracranial venous system","text":"Phenotype: Nonpyogenic thrombosis of intracranial venous system<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.909<br>N cases: 231<br>N controls: 342673"}
{"pvalue":0.653,"sign":1,"group":"I9: Circulatory system diseases","label":"Other embolism and thrombosis","text":"Phenotype: Other embolism and thrombosis<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.653<br>N cases: 3861<br>N controls: 324121"}
{"pvalue":0.732,"sign":-1,"group":"I9: Circulatory system diseases","label":"Transient ischemic attack","text":"Phenotype: Transient ischemic attack<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.732<br>N cases: 18398<br>N controls: 342294"}
{"pvalue":0.0215,"sign":-1,"group":"I9: Circulatory system diseases","label":"Unstable angina pectoris","text":"Phenotype: Unstable angina pectoris<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0215<br>N cases: 13304<br>N controls: 333375"}
{"pvalue":0.557,"sign":1,"group":"I9: Circulatory system diseases","label":"Varicose veins","text":"Phenotype: Varicose veins<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.557<br>N cases: 29539<br>N controls: 324121"}
{"pvalue":0.524,"sign":1,"group":"I9: Circulatory system diseases","label":"Oesophageal varices","text":"Phenotype: Oesophageal varices<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.524<br>N cases: 1017<br>N controls: 324121"}
{"pvalue":0.801,"sign":-1,"group":"I9: Circulatory system diseases","label":"Varicose veins of other sites","text":"Phenotype: Varicose veins of other sites<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.801<br>N cases: 1866<br>N controls: 324121"}
{"pvalue":0.162,"sign":1,"group":"I9: Circulatory system diseases","label":"Vascular diseases of the intestine","text":"Phenotype: Vascular diseases of the intestine<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.162<br>N cases: 966<br>N controls: 349539"}
{"pvalue":0.437,"sign":-1,"group":"I9: Circulatory system diseases","label":"Vascular syndromes of brain in cerebrovascular disorders","text":"Phenotype: Vascular syndromes of brain in cerebrovascular disorders<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.437<br>N cases: 1180<br>N controls: 359161"}
{"pvalue":0.119,"sign":-1,"group":"I9: Circulatory system diseases","label":"Other disorders of veins","text":"Phenotype: Other disorders of veins<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.119<br>N cases: 12630<br>N controls: 324121"}
{"pvalue":0.252,"sign":-1,"group":"I9: Circulatory system diseases","label":"Valvular heart disease excluding rheumatic fever","text":"Phenotype: Valvular heart disease excluding rheumatic fever<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.252<br>N cases: 20929<br>N controls: 286109"}
{"pvalue":0.374,"sign":1,"group":"I9: Circulatory system diseases","label":"Venous thromboembolism","text":"Phenotype: Venous thromboembolism<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.374<br>N cases: 19372<br>N controls: 357905"}
{"pvalue":0.844,"sign":1,"group":"N14: Genitourinary system diseases","label":"Interstitial cystitis (chronic), drug-induced","text":"Phenotype: Interstitial cystitis (chronic), drug-induced<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.844<br>N cases: 87<br>N controls: 377190"}
{"pvalue":0.182,"sign":-1,"group":"J10: Respiratory system diseases","label":"Abscess of lung","text":"Phenotype: Abscess of lung<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.182<br>N cases: 390<br>N controls: 375800"}
{"pvalue":0.478,"sign":-1,"group":"J10: Respiratory system diseases","label":"Unspecified acute lower respiratory infection","text":"Phenotype: Unspecified acute lower respiratory infection<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.478<br>N cases: 4616<br>N controls: 356404"}
{"pvalue":0.186,"sign":1,"group":"J10: Respiratory system diseases","label":"Acute upper respiratory infections of multiple and unspecified sites","text":"Phenotype: Acute upper respiratory infections of multiple and unspecified sites<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.186<br>N cases: 36445<br>N controls: 308166"}
{"pvalue":0.253,"sign":-1,"group":"J10: Respiratory system diseases","label":"Adult respiratory distress syndrome","text":"Phenotype: Adult respiratory distress syndrome<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.253<br>N cases: 328<br>N controls: 372077"}
{"pvalue":0.822,"sign":-1,"group":"J10: Respiratory system diseases","label":"Pneumoconiosis due to asbestos and other mineral fibres","text":"Phenotype: Pneumoconiosis due to asbestos and other mineral fibres<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.822<br>N cases: 610<br>N controls: 372962"}
{"pvalue":0.00111,"sign":1,"group":"J10: Respiratory system diseases","label":"Asthma/COPD (KELA code 203)","text":"Phenotype: Asthma/COPD (KELA code 203)<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00111<br>N cases: 41495<br>N controls: 311286"}
{"pvalue":0.00015,"sign":1,"group":"J10: Respiratory system diseases","label":"Asthma (more control exclusions)","text":"Phenotype: Asthma (more control exclusions)<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.000153<br>N cases: 42163<br>N controls: 202399"}
{"pvalue":0.00024,"sign":1,"group":"J10: Respiratory system diseases","label":"Asthma (only as main-diagnosis) (more control exclusions)","text":"Phenotype: Asthma (only as main-diagnosis) (more control exclusions)<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.000236<br>N cases: 34343<br>N controls: 202399"}
{"pvalue":0.134,"sign":1,"group":"J10: Respiratory system diseases","label":"Bronchitis, not specified as acute or chronic","text":"Phenotype: Bronchitis, not specified as acute or chronic<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.134<br>N cases: 2816<br>N controls: 311286"}
{"pvalue":0.772,"sign":-1,"group":"J10: Respiratory system diseases","label":"Bronchiectasis","text":"Phenotype: Bronchiectasis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.772<br>N cases: 2188<br>N controls: 311286"}
{"pvalue":0.0968,"sign":1,"group":"J10: Respiratory system diseases","label":"Acute bronchiolitis","text":"Phenotype: Acute bronchiolitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0968<br>N cases: 1953<br>N controls: 356404"}
{"pvalue":0.475,"sign":1,"group":"J10: Respiratory system diseases","label":"Acute bronchitis","text":"Phenotype: Acute bronchitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.475<br>N cases: 15393<br>N controls: 356404"}
{"pvalue":0.155,"sign":1,"group":"J10: Respiratory system diseases","label":"Unspecified chronic bronchitis","text":"Phenotype: Unspecified chronic bronchitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.155<br>N cases: 1150<br>N controls: 311286"}
{"pvalue":0.0102,"sign":1,"group":"J10: Respiratory system diseases","label":"Respiratory conditions due to inhalation of chemicals, gases, fumes and vapours","text":"Phenotype: Respiratory conditions due to inhalation of chemicals, gases, fumes and vapours<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0102<br>N cases: 233<br>N controls: 372962"}
{"pvalue":0.311,"sign":1,"group":"J10: Respiratory system diseases","label":"Chronic laryngitis and laryngotracheitis","text":"Phenotype: Chronic laryngitis and laryngotracheitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.311<br>N cases: 4319<br>N controls: 283342"}
{"pvalue":0.843,"sign":1,"group":"J10: Respiratory system diseases","label":"Chronic rhinitis, nasopharyngitis and pharyngitis","text":"Phenotype: Chronic rhinitis, nasopharyngitis and pharyngitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.843<br>N cases: 10868<br>N controls: 283342"}
{"pvalue":0.0815,"sign":1,"group":"J10: Respiratory system diseases","label":"Chronic sinusitis","text":"Phenotype: Chronic sinusitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0815<br>N cases: 16395<br>N controls: 283342"}
{"pvalue":0.00015,"sign":1,"group":"J10: Respiratory system diseases","label":"Chronic diseases of tonsils and adenoids","text":"Phenotype: Chronic diseases of tonsils and adenoids<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.000147<br>N cases: 43325<br>N controls: 283342"}
{"pvalue":0.81,"sign":1,"group":"J10: Respiratory system diseases","label":"Acute nasopharyngitis(common cold)","text":"Phenotype: Acute nasopharyngitis(common cold)<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.81<br>N cases: 3956<br>N controls: 308166"}
{"pvalue":0.159,"sign":1,"group":"J10: Respiratory system diseases","label":"COPD","text":"Phenotype: COPD<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.159<br>N cases: 18266<br>N controls: 311286"}
{"pvalue":0.335,"sign":1,"group":"J10: Respiratory system diseases","label":"Emphysema","text":"Phenotype: Emphysema<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.335<br>N cases: 1885<br>N controls: 311286"}
{"pvalue":0.51,"sign":-1,"group":"J10: Respiratory system diseases","label":"Acute epiglottitis","text":"Phenotype: Acute epiglottitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.51<br>N cases: 418<br>N controls: 308166"}
{"pvalue":0.554,"sign":1,"group":"J10: Respiratory system diseases","label":"Lung diseases due to external agents","text":"Phenotype: Lung diseases due to external agents<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.554<br>N cases: 4315<br>N controls: 372962"}
{"pvalue":0.118,"sign":-1,"group":"J10: Respiratory system diseases","label":"Hypersensitivity pneumonitis due to organic dust","text":"Phenotype: Hypersensitivity pneumonitis due to organic dust<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.118<br>N cases: 446<br>N controls: 372962"}
{"pvalue":0.0655,"sign":-1,"group":"J10: Respiratory system diseases","label":"All influenza","text":"Phenotype: All influenza<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0655<br>N cases: 8555<br>N controls: 314673"}
{"pvalue":0.34,"sign":1,"group":"J10: Respiratory system diseases","label":"Influenza and pneumonia","text":"Phenotype: Influenza and pneumonia<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.34<br>N cases: 62604<br>N controls: 314673"}
{"pvalue":0.729,"sign":-1,"group":"J10: Respiratory system diseases","label":"Pneumoconiosis due to other inorganic dusts","text":"Phenotype: Pneumoconiosis due to other inorganic dusts<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.729<br>N cases: 112<br>N controls: 372962"}
{"pvalue":0.00847,"sign":1,"group":"J10: Respiratory system diseases","label":"Acute laryngitis and tracheitis","text":"Phenotype: Acute laryngitis and tracheitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00847<br>N cases: 4158<br>N controls: 308166"}
{"pvalue":0.00008,"sign":1,"group":"J10: Respiratory system diseases","label":"Chronic lower respiratory diseases","text":"Phenotype: Chronic lower respiratory diseases<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 8.37e-05<br>N cases: 65991<br>N controls: 311286"}
{"pvalue":0.302,"sign":1,"group":"J10: Respiratory system diseases","label":"Other acute lower respiratory infections","text":"Phenotype: Other acute lower respiratory infections<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.302<br>N cases: 20873<br>N controls: 356404"}
{"pvalue":0.224,"sign":1,"group":"J10: Respiratory system diseases","label":"Nasal polyp","text":"Phenotype: Nasal polyp<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.224<br>N cases: 6255<br>N controls: 283342"}
{"pvalue":0.026,"sign":-1,"group":"J10: Respiratory system diseases","label":"Suppurative and necrotic conditions of lower respiratory tract","text":"Phenotype: Suppurative and necrotic conditions of lower respiratory tract<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.026<br>N cases: 1477<br>N controls: 375800"}
{"pvalue":0.00083,"sign":-1,"group":"J10: Respiratory system diseases","label":"Peritonsillar abscess","text":"Phenotype: Peritonsillar abscess<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.000834<br>N cases: 7510<br>N controls: 283342"}
{"pvalue":0.719,"sign":1,"group":"J10: Respiratory system diseases","label":"Acute pharyngitis","text":"Phenotype: Acute pharyngitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.719<br>N cases: 4747<br>N controls: 308166"}
{"pvalue":0.0178,"sign":1,"group":"J10: Respiratory system diseases","label":"Other diseases of pleura","text":"Phenotype: Other diseases of pleura<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0178<br>N cases: 15441<br>N controls: 361836"}
{"pvalue":0.0332,"sign":1,"group":"J10: Respiratory system diseases","label":"Pleural effusion","text":"Phenotype: Pleural effusion<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0332<br>N cases: 4513<br>N controls: 361836"}
{"pvalue":0.00759,"sign":1,"group":"J10: Respiratory system diseases","label":"Other pleural conditions","text":"Phenotype: Other pleural conditions<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00759<br>N cases: 2985<br>N controls: 361836"}
{"pvalue":0.42,"sign":1,"group":"J10: Respiratory system diseases","label":"Pleural plaque","text":"Phenotype: Pleural plaque<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.42<br>N cases: 2819<br>N controls: 361836"}
{"pvalue":0.0197,"sign":1,"group":"J10: Respiratory system diseases","label":"Bacterial pneumoniae","text":"Phenotype: Bacterial pneumoniae<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0197<br>N cases: 16244<br>N controls: 314673"}
{"pvalue":0.0174,"sign":1,"group":"J10: Respiratory system diseases","label":"Pneumonia due to Haemophilus influenzae","text":"Phenotype: Pneumonia due to Haemophilus influenzae<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0174<br>N cases: 87<br>N controls: 314673"}
{"pvalue":0.0629,"sign":1,"group":"J10: Respiratory system diseases","label":"All pneumoniae","text":"Phenotype: All pneumoniae<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0629<br>N cases: 58174<br>N controls: 319103"}
{"pvalue":0.676,"sign":1,"group":"J10: Respiratory system diseases","label":"Pneumonitis due to solids and liquids","text":"Phenotype: Pneumonitis due to solids and liquids<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.676<br>N cases: 2326<br>N controls: 372962"}
{"pvalue":0.153,"sign":-1,"group":"J10: Respiratory system diseases","label":"Pneumonia due to other infectious organisms, not elsewhere classified","text":"Phenotype: Pneumonia due to other infectious organisms, not elsewhere classified<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.153<br>N cases: 830<br>N controls: 314673"}
{"pvalue":0.605,"sign":1,"group":"J10: Respiratory system diseases","label":"Pneumonia due to Streptococcus pneumoniae","text":"Phenotype: Pneumonia due to Streptococcus pneumoniae<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.605<br>N cases: 1245<br>N controls: 314673"}
{"pvalue":0.795,"sign":-1,"group":"J10: Respiratory system diseases","label":"Pneumothorax","text":"Phenotype: Pneumothorax<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.795<br>N cases: 1999<br>N controls: 361836"}
{"pvalue":0.129,"sign":1,"group":"J10: Respiratory system diseases","label":"Pulmonary eosinophilia, not elsewhere classified","text":"Phenotype: Pulmonary eosinophilia, not elsewhere classified<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.129<br>N cases: 324<br>N controls: 372077"}
{"pvalue":0.716,"sign":-1,"group":"J10: Respiratory system diseases","label":"Pulmonary oedema","text":"Phenotype: Pulmonary oedema<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.716<br>N cases: 477<br>N controls: 372077"}
{"pvalue":0.011,"sign":-1,"group":"J10: Respiratory system diseases","label":"Pyothorax","text":"Phenotype: Pyothorax<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.011<br>N cases: 1120<br>N controls: 375800"}
{"pvalue":0.67,"sign":1,"group":"J10: Respiratory system diseases","label":"Respiratory conditions due to other external agents","text":"Phenotype: Respiratory conditions due to other external agents<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.67<br>N cases: 510<br>N controls: 372962"}
{"pvalue":0.489,"sign":1,"group":"J10: Respiratory system diseases","label":"Other diseases of the respiratory system","text":"Phenotype: Other diseases of the respiratory system<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.489<br>N cases: 6381<br>N controls: 370896"}
{"pvalue":0.541,"sign":1,"group":"J10: Respiratory system diseases","label":"Deviated nasal septum","text":"Phenotype: Deviated nasal septum<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.541<br>N cases: 11680<br>N controls: 283342"}
{"pvalue":0.194,"sign":1,"group":"J10: Respiratory system diseases","label":"Pneumoconiosis due to dust containing silica","text":"Phenotype: Pneumoconiosis due to dust containing silica<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.194<br>N cases: 92<br>N controls: 372962"}
{"pvalue":0.208,"sign":-1,"group":"J10: Respiratory system diseases","label":"Simple and mucopurulent chronic bronchitis","text":"Phenotype: Simple and mucopurulent chronic bronchitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.208<br>N cases: 1299<br>N controls: 311286"}
{"pvalue":0.325,"sign":1,"group":"J10: Respiratory system diseases","label":"Acute sinusitis","text":"Phenotype: Acute sinusitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.325<br>N cases: 20520<br>N controls: 308166"}
{"pvalue":0.108,"sign":1,"group":"J10: Respiratory system diseases","label":"Tonsillectomy","text":"Phenotype: Tonsillectomy<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.108<br>N cases: 27449<br>N controls: 349828"}
{"pvalue":0.164,"sign":-1,"group":"J10: Respiratory system diseases","label":"Other and unspecified tonsillitis","text":"Phenotype: Other and unspecified tonsillitis<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.164<br>N cases: 13190<br>N controls: 308166"}
{"pvalue":0.00339,"sign":1,"group":"J10: Respiratory system diseases","label":"Other diseases of upper respiratory tract","text":"Phenotype: Other diseases of upper respiratory tract<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00339<br>N cases: 93935<br>N controls: 283342"}
{"pvalue":0.334,"sign":1,"group":"J10: Respiratory system diseases","label":"Acute upper respiratory infections","text":"Phenotype: Acute upper respiratory infections<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.334<br>N cases: 69111<br>N controls: 308166"}
{"pvalue":0.281,"sign":1,"group":"J10: Respiratory system diseases","label":"Viral pneumonia","text":"Phenotype: Viral pneumonia<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.281<br>N cases: 3394<br>N controls: 314673"}
{"pvalue":0.141,"sign":1,"group":"J10: Respiratory system diseases","label":"Diseases of vocal cords and larynx+other diseases of upper respiratory tract, no elsewhere classified","text":"Phenotype: Diseases of vocal cords and larynx+other diseases of upper respiratory tract, no elsewhere classified<br>Category: J10: Respiratory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.141<br>N cases: 19530<br>N controls: 283342"}
{"pvalue":0.895,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Pain in joint","text":"Phenotype: Pain in joint<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.895<br>N cases: 27688<br>N controls: 205355"}
{"pvalue":0.453,"sign":1,"group":"K11: Digestive system diseases","label":"Abrasion of teeth","text":"Phenotype: Abrasion of teeth<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.453<br>N cases: 149<br>N controls: 259234"}
{"pvalue":0.463,"sign":1,"group":"K11: Digestive system diseases","label":"Abscess of anal and rectal regions","text":"Phenotype: Abscess of anal and rectal regions<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.463<br>N cases: 2595<br>N controls: 301931"}
{"pvalue":0.204,"sign":1,"group":"K11: Digestive system diseases","label":"Achalasia of cardia","text":"Phenotype: Achalasia of cardia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.204<br>N cases: 506<br>N controls: 320387"}
{"pvalue":0.896,"sign":-1,"group":"K11: Digestive system diseases","label":"Acute gastritis","text":"Phenotype: Acute gastritis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.896<br>N cases: 2370<br>N controls: 320387"}
{"pvalue":0.107,"sign":1,"group":"K11: Digestive system diseases","label":"Acute pancreatitis","text":"Phenotype: Acute pancreatitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.107<br>N cases: 6223<br>N controls: 330903"}
{"pvalue":0.0409,"sign":1,"group":"K11: Digestive system diseases","label":"Intestinal adhesions without obstruction","text":"Phenotype: Intestinal adhesions without obstruction<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0409<br>N cases: 2370<br>N controls: 301931"}
{"pvalue":0.0261,"sign":1,"group":"K11: Digestive system diseases","label":"Alcoholic gastritis","text":"Phenotype: Alcoholic gastritis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0261<br>N cases: 430<br>N controls: 320387"}
{"pvalue":0.768,"sign":1,"group":"K11: Digestive system diseases","label":"Alcoholic liver disease","text":"Phenotype: Alcoholic liver disease<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.768<br>N cases: 2761<br>N controls: 366450"}
{"pvalue":0.0218,"sign":-1,"group":"K11: Digestive system diseases","label":"Anomalies of dental arch relationship, including avohilmo","text":"Phenotype: Anomalies of dental arch relationship, including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0218<br>N cases: 6260<br>N controls: 371017"}
{"pvalue":0.632,"sign":-1,"group":"K11: Digestive system diseases","label":"Recurring oral aphthae","text":"Phenotype: Recurring oral aphthae<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.632<br>N cases: 1221<br>N controls: 376056"}
{"pvalue":0.184,"sign":-1,"group":"K11: Digestive system diseases","label":"Recurring oral aphthae, including avohilmo","text":"Phenotype: Recurring oral aphthae, including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.184<br>N cases: 3577<br>N controls: 373700"}
{"pvalue":0.069,"sign":1,"group":"K11: Digestive system diseases","label":"Acute appendicitis","text":"Phenotype: Acute appendicitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.069<br>N cases: 28745<br>N controls: 346283"}
{"pvalue":0.225,"sign":1,"group":"K11: Digestive system diseases","label":"Appendectomy","text":"Phenotype: Appendectomy<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.225<br>N cases: 26013<br>N controls: 351264"}
{"pvalue":0.773,"sign":-1,"group":"K11: Digestive system diseases","label":"Other appendicitis","text":"Phenotype: Other appendicitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.773<br>N cases: 2545<br>N controls: 346283"}
{"pvalue":0.831,"sign":1,"group":"K11: Digestive system diseases","label":"Asymmetry of jaw","text":"Phenotype: Asymmetry of jaw<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.831<br>N cases: 369<br>N controls: 376908"}
{"pvalue":0.251,"sign":1,"group":"K11: Digestive system diseases","label":"Excessive attrition of teeth","text":"Phenotype: Excessive attrition of teeth<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.251<br>N cases: 840<br>N controls: 259234"}
{"pvalue":0.121,"sign":-1,"group":"K11: Digestive system diseases","label":"Barrett oesophagus","text":"Phenotype: Barrett oesophagus<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.121<br>N cases: 1123<br>N controls: 320387"}
{"pvalue":0.513,"sign":1,"group":"K11: Digestive system diseases","label":"Other diseases of biliary tract","text":"Phenotype: Other diseases of biliary tract<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.513<br>N cases: 2294<br>N controls: 330903"}
{"pvalue":0.232,"sign":-1,"group":"K11: Digestive system diseases","label":"Dental caries 1, only avohilmo","text":"Phenotype: Dental caries 1, only avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.232<br>N cases: 161113<br>N controls: 216164"}
{"pvalue":0.887,"sign":1,"group":"K11: Digestive system diseases","label":"Dental caries 2","text":"Phenotype: Dental caries 2<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.887<br>N cases: 25095<br>N controls: 352182"}
{"pvalue":0.577,"sign":1,"group":"K11: Digestive system diseases","label":"Dentinal caries","text":"Phenotype: Dentinal caries<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.577<br>N cases: 7680<br>N controls: 259234"}
{"pvalue":0.658,"sign":1,"group":"K11: Digestive system diseases","label":"Crohn disease (strict definition, require KELA, min 2 HDR)","text":"Phenotype: Crohn disease (strict definition, require KELA, min 2 HDR)<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.658<br>N cases: 1665<br>N controls: 375445"}
{"pvalue":0.504,"sign":-1,"group":"K11: Digestive system diseases","label":"Cholangitis (primary sclerosing, PSC)","text":"Phenotype: Cholangitis (primary sclerosing, PSC)<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.504<br>N cases: 1715<br>N controls: 330903"}
{"pvalue":0.00146,"sign":1,"group":"K11: Digestive system diseases","label":"Cholecystectomy","text":"Phenotype: Cholecystectomy<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00146<br>N cases: 26778<br>N controls: 350499"}
{"pvalue":0.968,"sign":-1,"group":"K11: Digestive system diseases","label":"Cholecystitis","text":"Phenotype: Cholecystitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.968<br>N cases: 4299<br>N controls: 330903"}
{"pvalue":0.00064,"sign":1,"group":"K11: Digestive system diseases","label":"Cholelithiasis","text":"Phenotype: Cholelithiasis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.000638<br>N cases: 37041<br>N controls: 330903"}
{"pvalue":0.296,"sign":-1,"group":"K11: Digestive system diseases","label":"Chronic gastritis","text":"Phenotype: Chronic gastritis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.296<br>N cases: 9570<br>N controls: 320387"}
{"pvalue":0.569,"sign":1,"group":"K11: Digestive system diseases","label":"Chronic hepatitis, not elsewhere classified","text":"Phenotype: Chronic hepatitis, not elsewhere classified<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.569<br>N cases: 885<br>N controls: 366450"}
{"pvalue":0.0437,"sign":1,"group":"K11: Digestive system diseases","label":"Chronic pancreatitis","text":"Phenotype: Chronic pancreatitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0437<br>N cases: 3320<br>N controls: 330903"}
{"pvalue":0.567,"sign":-1,"group":"K11: Digestive system diseases","label":"Coeliac disease","text":"Phenotype: Coeliac disease<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.567<br>N cases: 3690<br>N controls: 361055"}
{"pvalue":0.531,"sign":-1,"group":"K11: Digestive system diseases","label":"Constipation","text":"Phenotype: Constipation<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.531<br>N cases: 36022<br>N controls: 341255"}
{"pvalue":0.00834,"sign":-1,"group":"K11: Digestive system diseases","label":"Crossbite","text":"Phenotype: Crossbite<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00834<br>N cases: 1678<br>N controls: 375599"}
{"pvalue":0.316,"sign":-1,"group":"K11: Digestive system diseases","label":"Crowding of teeth, including avohilmo","text":"Phenotype: Crowding of teeth, including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.316<br>N cases: 2468<br>N controls: 374809"}
{"pvalue":0.512,"sign":-1,"group":"K11: Digestive system diseases","label":"Deep bite , including avohilmo","text":"Phenotype: Deep bite , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.512<br>N cases: 2804<br>N controls: 374473"}
{"pvalue":0.572,"sign":-1,"group":"K11: Digestive system diseases","label":"Deep bite that required surgery","text":"Phenotype: Deep bite that required surgery<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.572<br>N cases: 293<br>N controls: 376984"}
{"pvalue":0.618,"sign":-1,"group":"K11: Digestive system diseases","label":"Dentofacial anomalies [including malocclusion]","text":"Phenotype: Dentofacial anomalies [including malocclusion]<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.618<br>N cases: 9866<br>N controls: 259234"}
{"pvalue":0.236,"sign":-1,"group":"K11: Digestive system diseases","label":"Deposits [accretions] on teeth","text":"Phenotype: Deposits [accretions] on teeth<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.236<br>N cases: 1974<br>N controls: 259234"}
{"pvalue":0.0333,"sign":1,"group":"K11: Digestive system diseases","label":"Diaphragmatic hernia","text":"Phenotype: Diaphragmatic hernia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0333<br>N cases: 11757<br>N controls: 322586"}
{"pvalue":0.877,"sign":-1,"group":"K11: Digestive system diseases","label":"Other diseases of liver","text":"Phenotype: Other diseases of liver<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.877<br>N cases: 5052<br>N controls: 366450"}
{"pvalue":0.899,"sign":1,"group":"K11: Digestive system diseases","label":"Disorders of oesophagus in diseases classified elsewhere","text":"Phenotype: Disorders of oesophagus in diseases classified elsewhere<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.899<br>N cases: 523<br>N controls: 320387"}
{"pvalue":0.522,"sign":1,"group":"K11: Digestive system diseases","label":"Other disorders of teeth and supporting structures","text":"Phenotype: Other disorders of teeth and supporting structures<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.522<br>N cases: 6850<br>N controls: 259234"}
{"pvalue":0.224,"sign":-1,"group":"K11: Digestive system diseases","label":"Distal bite , including avohilmo","text":"Phenotype: Distal bite , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.224<br>N cases: 771<br>N controls: 376506"}
{"pvalue":0.917,"sign":1,"group":"K11: Digestive system diseases","label":"Diverticular disease of intestine","text":"Phenotype: Diverticular disease of intestine<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.917<br>N cases: 30649<br>N controls: 301931"}
{"pvalue":0.751,"sign":1,"group":"K11: Digestive system diseases","label":"Duodenal ulcer","text":"Phenotype: Duodenal ulcer<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.751<br>N cases: 3520<br>N controls: 320387"}
{"pvalue":0.838,"sign":1,"group":"K11: Digestive system diseases","label":"Embedded teeth, including avohilmo","text":"Phenotype: Embedded teeth, including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.838<br>N cases: 2429<br>N controls: 374848"}
{"pvalue":0.459,"sign":-1,"group":"K11: Digestive system diseases","label":"Embedded and impacted teeth , including avohilmo","text":"Phenotype: Embedded and impacted teeth , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.459<br>N cases: 8139<br>N controls: 369138"}
{"pvalue":0.655,"sign":-1,"group":"K11: Digestive system diseases","label":"Noninfective enteritis and colitis","text":"Phenotype: Noninfective enteritis and colitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.655<br>N cases: 17350<br>N controls: 359927"}
{"pvalue":0.842,"sign":1,"group":"K11: Digestive system diseases","label":"Erosion of teeth","text":"Phenotype: Erosion of teeth<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.842<br>N cases: 425<br>N controls: 259234"}
{"pvalue":0.0218,"sign":1,"group":"K11: Digestive system diseases","label":"Erosion of teeth, including avohilmo","text":"Phenotype: Erosion of teeth, including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0218<br>N cases: 5521<br>N controls: 371756"}
{"pvalue":0.394,"sign":1,"group":"K11: Digestive system diseases","label":"Tooth eruption problems , including avohilmo","text":"Phenotype: Tooth eruption problems , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.394<br>N cases: 3805<br>N controls: 373472"}
{"pvalue":0.844,"sign":1,"group":"K11: Digestive system diseases","label":"Femoral hernia","text":"Phenotype: Femoral hernia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.844<br>N cases: 1267<br>N controls: 322586"}
{"pvalue":0.325,"sign":-1,"group":"K11: Digestive system diseases","label":"Fibrosis and cirrhosis of liver","text":"Phenotype: Fibrosis and cirrhosis of liver<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.325<br>N cases: 1841<br>N controls: 366450"}
{"pvalue":0.911,"sign":-1,"group":"K11: Digestive system diseases","label":"Colonic or urogenital fistula","text":"Phenotype: Colonic or urogenital fistula<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.911<br>N cases: 8879<br>N controls: 368398"}
{"pvalue":0.636,"sign":1,"group":"K11: Digestive system diseases","label":"Functional dyspepsia","text":"Phenotype: Functional dyspepsia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.636<br>N cases: 8875<br>N controls: 320387"}
{"pvalue":0.269,"sign":1,"group":"K11: Digestive system diseases","label":"Other diseases of gallbladder","text":"Phenotype: Other diseases of gallbladder<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.269<br>N cases: 1200<br>N controls: 330903"}
{"pvalue":0.465,"sign":1,"group":"K11: Digestive system diseases","label":"Gastroduodenal ulcer","text":"Phenotype: Gastroduodenal ulcer<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.465<br>N cases: 9216<br>N controls: 320387"}
{"pvalue":0.0289,"sign":-1,"group":"K11: Digestive system diseases","label":"Other disorders of gingiva or/and edentulous alveolar ridge","text":"Phenotype: Other disorders of gingiva or/and edentulous alveolar ridge<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0289<br>N cases: 899<br>N controls: 259234"}
{"pvalue":0.0652,"sign":-1,"group":"K11: Digestive system diseases","label":"Gingival hyperplasia","text":"Phenotype: Gingival hyperplasia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0652<br>N cases: 379<br>N controls: 259234"}
{"pvalue":0.898,"sign":1,"group":"K11: Digestive system diseases","label":"Gingivitis and periodontal diseases","text":"Phenotype: Gingivitis and periodontal diseases<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.898<br>N cases: 87497<br>N controls: 259234"}
{"pvalue":0.115,"sign":-1,"group":"K11: Digestive system diseases","label":"Gastrojejunal ulcer","text":"Phenotype: Gastrojejunal ulcer<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.115<br>N cases: 324<br>N controls: 320387"}
{"pvalue":0.145,"sign":1,"group":"K11: Digestive system diseases","label":"Gastric ulcer","text":"Phenotype: Gastric ulcer<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.145<br>N cases: 5935<br>N controls: 320387"}
{"pvalue":0.2,"sign":-1,"group":"K11: Digestive system diseases","label":"Haemmorrhoids and perianal venous thrombosis","text":"Phenotype: Haemmorrhoids and perianal venous thrombosis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.2<br>N cases: 8583<br>N controls: 301931"}
{"pvalue":0.764,"sign":1,"group":"K11: Digestive system diseases","label":"Hepatic failure, not elsewhere classified","text":"Phenotype: Hepatic failure, not elsewhere classified<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.764<br>N cases: 948<br>N controls: 366450"}
{"pvalue":0.723,"sign":1,"group":"K11: Digestive system diseases","label":"Inguinal hernia","text":"Phenotype: Inguinal hernia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.723<br>N cases: 32335<br>N controls: 322586"}
{"pvalue":0.182,"sign":1,"group":"K11: Digestive system diseases","label":"Hernia","text":"Phenotype: Hernia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.182<br>N cases: 54691<br>N controls: 322586"}
{"pvalue":0.682,"sign":1,"group":"K11: Digestive system diseases","label":"Hypertrophy of tongue papillae","text":"Phenotype: Hypertrophy of tongue papillae<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.682<br>N cases: 268<br>N controls: 377009"}
{"pvalue":0.253,"sign":-1,"group":"K11: Digestive system diseases","label":"Hypoplasia of dental enamel","text":"Phenotype: Hypoplasia of dental enamel<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.253<br>N cases: 218<br>N controls: 376688"}
{"pvalue":0.118,"sign":1,"group":"K11: Digestive system diseases","label":"Tooth agenesis EXCLUDE clefts and syndromes , including avohilmo","text":"Phenotype: Tooth agenesis EXCLUDE clefts and syndromes , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.118<br>N cases: 920<br>N controls: 375469"}
{"pvalue":0.0819,"sign":-1,"group":"K11: Digestive system diseases","label":"Hypoplasia of dental enamel , including avohilmo","text":"Phenotype: Hypoplasia of dental enamel , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0819<br>N cases: 540<br>N controls: 376737"}
{"pvalue":0.161,"sign":-1,"group":"K11: Digestive system diseases","label":"Hypoplasia of dental enamel, prenatal , including avohilmo","text":"Phenotype: Hypoplasia of dental enamel, prenatal , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.161<br>N cases: 94<br>N controls: 377183"}
{"pvalue":0.98,"sign":-1,"group":"K11: Digestive system diseases","label":"Inflammatory bowel disease, strict (require KELA)","text":"Phenotype: Inflammatory bowel disease, strict (require KELA)<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.98<br>N cases: 7625<br>N controls: 369652"}
{"pvalue":0.922,"sign":1,"group":"K11: Digestive system diseases","label":"Irritable bowel syndrome","text":"Phenotype: Irritable bowel syndrome<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.922<br>N cases: 9323<br>N controls: 301931"}
{"pvalue":0.0419,"sign":1,"group":"K11: Digestive system diseases","label":"Paralytic ileus and intestinal obstruction","text":"Phenotype: Paralytic ileus and intestinal obstruction<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0419<br>N cases: 8660<br>N controls: 301931"}
{"pvalue":0.472,"sign":-1,"group":"K11: Digestive system diseases","label":"Impacted teeth , including avohilmo","text":"Phenotype: Impacted teeth , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.472<br>N cases: 5435<br>N controls: 371842"}
{"pvalue":0.97,"sign":-1,"group":"K11: Digestive system diseases","label":"Impaction of intestines","text":"Phenotype: Impaction of intestines<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.97<br>N cases: 189<br>N controls: 301931"}
{"pvalue":0.927,"sign":1,"group":"K11: Digestive system diseases","label":"Other diseases of intestines","text":"Phenotype: Other diseases of intestines<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.927<br>N cases: 75346<br>N controls: 301931"}
{"pvalue":0.244,"sign":1,"group":"K11: Digestive system diseases","label":"Intussusception","text":"Phenotype: Intussusception<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.244<br>N cases: 555<br>N controls: 301931"}
{"pvalue":0.758,"sign":-1,"group":"K11: Digestive system diseases","label":"Other diseases of jaws","text":"Phenotype: Other diseases of jaws<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.758<br>N cases: 1958<br>N controls: 259234"}
{"pvalue":0.968,"sign":-1,"group":"K11: Digestive system diseases","label":"IBD patients in KELA-register","text":"Phenotype: IBD patients in KELA-register<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.968<br>N cases: 7625<br>N controls: 359927"}
{"pvalue":0.692,"sign":-1,"group":"K11: Digestive system diseases","label":"Other diseases of lip and oral mucosa","text":"Phenotype: Other diseases of lip and oral mucosa<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.692<br>N cases: 4895<br>N controls: 259234"}
{"pvalue":0.642,"sign":-1,"group":"K11: Digestive system diseases","label":"Diseases of liver","text":"Phenotype: Diseases of liver<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.642<br>N cases: 10827<br>N controls: 366450"}
{"pvalue":0.342,"sign":1,"group":"K11: Digestive system diseases","label":"Major anomalies of jaw size , including avohilmo","text":"Phenotype: Major anomalies of jaw size , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.342<br>N cases: 719<br>N controls: 376558"}
{"pvalue":0.25,"sign":1,"group":"K11: Digestive system diseases","label":"Intestinal malabsorption","text":"Phenotype: Intestinal malabsorption<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.25<br>N cases: 1228<br>N controls: 361055"}
{"pvalue":0.377,"sign":-1,"group":"K11: Digestive system diseases","label":"Mandibular hypoplasia","text":"Phenotype: Mandibular hypoplasia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.377<br>N cases: 166<br>N controls: 377111"}
{"pvalue":0.388,"sign":-1,"group":"K11: Digestive system diseases","label":"Impacted maxillary canine","text":"Phenotype: Impacted maxillary canine<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.388<br>N cases: 183<br>N controls: 377094"}
{"pvalue":0.117,"sign":-1,"group":"K11: Digestive system diseases","label":"Palatinal maxillary canine","text":"Phenotype: Palatinal maxillary canine<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.117<br>N cases: 154<br>N controls: 377123"}
{"pvalue":0.12,"sign":1,"group":"K11: Digestive system diseases","label":"Impacted maxillary molar","text":"Phenotype: Impacted maxillary molar<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.12<br>N cases: 1375<br>N controls: 375902"}
{"pvalue":0.018,"sign":-1,"group":"K11: Digestive system diseases","label":"Maxillary prognathism","text":"Phenotype: Maxillary prognathism<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.018<br>N cases: 105<br>N controls: 377172"}
{"pvalue":0.817,"sign":-1,"group":"K11: Digestive system diseases","label":"Mesial bite","text":"Phenotype: Mesial bite<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.817<br>N cases: 219<br>N controls: 377058"}
{"pvalue":0.0107,"sign":-1,"group":"K11: Digestive system diseases","label":"Molar incisor enamel hypoplasia, with caries","text":"Phenotype: Molar incisor enamel hypoplasia, with caries<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0107<br>N cases: 187<br>N controls: 368407"}
{"pvalue":0.0929,"sign":-1,"group":"K11: Digestive system diseases","label":"Molar incisor enamel hypoplasia , including avohilmo","text":"Phenotype: Molar incisor enamel hypoplasia , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0929<br>N cases: 589<br>N controls: 376688"}
{"pvalue":0.827,"sign":1,"group":"K11: Digestive system diseases","label":"Missing teeth due to accident, extraction or parodontitis","text":"Phenotype: Missing teeth due to accident, extraction or parodontitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.827<br>N cases: 3291<br>N controls: 259234"}
{"pvalue":0.593,"sign":1,"group":"K11: Digestive system diseases","label":"Mandibular prognathia AND surgery (LeFortI or BSSRO)","text":"Phenotype: Mandibular prognathia AND surgery (LeFortI or BSSRO)<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.593<br>N cases: 118<br>N controls: 377064"}
{"pvalue":0.523,"sign":1,"group":"K11: Digestive system diseases","label":"Mandibular prognathia AND surgery (LeFortI or BSSO or LeFortI AND BSSO) , including avohilmo","text":"Phenotype: Mandibular prognathia AND surgery (LeFortI or BSSO or LeFortI AND BSSO) , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.523<br>N cases: 213<br>N controls: 377064"}
{"pvalue":0.966,"sign":-1,"group":"K11: Digestive system diseases","label":"Mandibular prognathia , including avohilmo","text":"Phenotype: Mandibular prognathia , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.966<br>N cases: 347<br>N controls: 376930"}
{"pvalue":0.714,"sign":-1,"group":"K11: Digestive system diseases","label":"Mandibular retrognathia AND surgery (BSSRO)","text":"Phenotype: Mandibular retrognathia AND surgery (BSSRO)<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.714<br>N cases: 666<br>N controls: 376611"}
{"pvalue":0.754,"sign":-1,"group":"K11: Digestive system diseases","label":"Mandibular retrognathia","text":"Phenotype: Mandibular retrognathia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.754<br>N cases: 1703<br>N controls: 375574"}
{"pvalue":0.46,"sign":-1,"group":"K11: Digestive system diseases","label":"Oesophagitis","text":"Phenotype: Oesophagitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.46<br>N cases: 1520<br>N controls: 320387"}
{"pvalue":0.523,"sign":1,"group":"K11: Digestive system diseases","label":"Oesophageal obstruction","text":"Phenotype: Oesophageal obstruction<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.523<br>N cases: 993<br>N controls: 320387"}
{"pvalue":0.218,"sign":1,"group":"K11: Digestive system diseases","label":"Diseases of oesophagus, stomach and duodenum","text":"Phenotype: Diseases of oesophagus, stomach and duodenum<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.218<br>N cases: 56890<br>N controls: 320387"}
{"pvalue":0.436,"sign":-1,"group":"K11: Digestive system diseases","label":"Ulcer of oesophagus, drug-induced","text":"Phenotype: Ulcer of oesophagus, drug-induced<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.436<br>N cases: 137<br>N controls: 377140"}
{"pvalue":0.613,"sign":-1,"group":"K11: Digestive system diseases","label":"Ulcer of oesophagus","text":"Phenotype: Ulcer of oesophagus<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.613<br>N cases: 2064<br>N controls: 320387"}
{"pvalue":0.885,"sign":-1,"group":"K11: Digestive system diseases","label":"Open bite , including avohilmo","text":"Phenotype: Open bite , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.885<br>N cases: 1255<br>N controls: 376022"}
{"pvalue":0.0664,"sign":-1,"group":"K11: Digestive system diseases","label":"Open bite that required surgery (Lefort1 or BSSRO)","text":"Phenotype: Open bite that required surgery (Lefort1 or BSSRO)<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0664<br>N cases: 237<br>N controls: 377040"}
{"pvalue":0.952,"sign":-1,"group":"K11: Digestive system diseases","label":"Cysts of oral region, not elsewhere classified","text":"Phenotype: Cysts of oral region, not elsewhere classified<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.952<br>N cases: 1223<br>N controls: 259234"}
{"pvalue":0.654,"sign":1,"group":"K11: Digestive system diseases","label":"Diseases of oral cavity, salivary glands and jaws","text":"Phenotype: Diseases of oral cavity, salivary glands and jaws<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.654<br>N cases: 118043<br>N controls: 259234"}
{"pvalue":0.0331,"sign":-1,"group":"K11: Digestive system diseases","label":"Oral leukoplakia","text":"Phenotype: Oral leukoplakia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0331<br>N cases: 474<br>N controls: 376803"}
{"pvalue":0.171,"sign":-1,"group":"K11: Digestive system diseases","label":"Oral leukoplakia, including avohilmo","text":"Phenotype: Oral leukoplakia, including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.171<br>N cases: 686<br>N controls: 376591"}
{"pvalue":0.895,"sign":1,"group":"K11: Digestive system diseases","label":"Oral leukoplakia and related diseases","text":"Phenotype: Oral leukoplakia and related diseases<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.895<br>N cases: 1531<br>N controls: 375746"}
{"pvalue":0.955,"sign":-1,"group":"K11: Digestive system diseases","label":"Oral leukoplakia and related diseases, including avohilmo","text":"Phenotype: Oral leukoplakia and related diseases, including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.955<br>N cases: 2382<br>N controls: 374895"}
{"pvalue":0.327,"sign":1,"group":"K11: Digestive system diseases","label":"Oral lichen ruber planus, hypothyreosis or thyroxin","text":"Phenotype: Oral lichen ruber planus, hypothyreosis or thyroxin<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.327<br>N cases: 327<br>N controls: 376950"}
{"pvalue":0.175,"sign":1,"group":"K11: Digestive system diseases","label":"Oral lichen ruber planus","text":"Phenotype: Oral lichen ruber planus<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.175<br>N cases: 510<br>N controls: 376767"}
{"pvalue":0.0232,"sign":1,"group":"K11: Digestive system diseases","label":"Oral lichen ruber planus, including avohilmo","text":"Phenotype: Oral lichen ruber planus, including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0232<br>N cases: 1319<br>N controls: 375958"}
{"pvalue":0.193,"sign":1,"group":"K11: Digestive system diseases","label":"Oral lichen ruber planus, wide definition","text":"Phenotype: Oral lichen ruber planus, wide definition<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.193<br>N cases: 5791<br>N controls: 371486"}
{"pvalue":0.3,"sign":-1,"group":"K11: Digestive system diseases","label":"Oral lichen ruber planus wide, hypothyreosis or thyroxin","text":"Phenotype: Oral lichen ruber planus wide, hypothyreosis or thyroxin<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.3<br>N cases: 1268<br>N controls: 376009"}
{"pvalue":0.00613,"sign":1,"group":"K11: Digestive system diseases","label":"Other and unspecified abdominal hernia","text":"Phenotype: Other and unspecified abdominal hernia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00613<br>N cases: 1088<br>N controls: 322586"}
{"pvalue":0.755,"sign":1,"group":"K11: Digestive system diseases","label":"Other diseases of anus and rectum","text":"Phenotype: Other diseases of anus and rectum<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.755<br>N cases: 9932<br>N controls: 301931"}
{"pvalue":0.455,"sign":-1,"group":"K11: Digestive system diseases","label":"Other diseases of appendix","text":"Phenotype: Other diseases of appendix<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.455<br>N cases: 303<br>N controls: 346283"}
{"pvalue":0.348,"sign":1,"group":"K11: Digestive system diseases","label":"Other diseases of the digestive system","text":"Phenotype: Other diseases of the digestive system<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.348<br>N cases: 16222<br>N controls: 361055"}
{"pvalue":0.342,"sign":1,"group":"K11: Digestive system diseases","label":"Other diseases of the digestive system","text":"Phenotype: Other diseases of the digestive system<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.342<br>N cases: 10589<br>N controls: 361055"}
{"pvalue":0.953,"sign":-1,"group":"K11: Digestive system diseases","label":"Other diseases of oesophagus","text":"Phenotype: Other diseases of oesophagus<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.953<br>N cases: 2936<br>N controls: 320387"}
{"pvalue":0.662,"sign":1,"group":"K11: Digestive system diseases","label":"Other diseases of stomach and duodenum","text":"Phenotype: Other diseases of stomach and duodenum<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.662<br>N cases: 1806<br>N controls: 320387"}
{"pvalue":0.66,"sign":1,"group":"K11: Digestive system diseases","label":"Other noninfective gastroenteritis and colitis","text":"Phenotype: Other noninfective gastroenteritis and colitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.66<br>N cases: 7988<br>N controls: 359927"}
{"pvalue":0.563,"sign":1,"group":"K11: Digestive system diseases","label":"Other functional intestinal disorders","text":"Phenotype: Other functional intestinal disorders<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.563<br>N cases: 16311<br>N controls: 301931"}
{"pvalue":0.778,"sign":1,"group":"K11: Digestive system diseases","label":"Other gastritis (incl. Duodenitis)","text":"Phenotype: Other gastritis (incl. Duodenitis)<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.778<br>N cases: 7514<br>N controls: 320387"}
{"pvalue":0.0837,"sign":1,"group":"K11: Digestive system diseases","label":"Other or unspecified ileus, impaction or obstruction","text":"Phenotype: Other or unspecified ileus, impaction or obstruction<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0837<br>N cases: 5925<br>N controls: 301931"}
{"pvalue":0.695,"sign":1,"group":"K11: Digestive system diseases","label":"Other inflammatory liver diseases","text":"Phenotype: Other inflammatory liver diseases<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.695<br>N cases: 1821<br>N controls: 366450"}
{"pvalue":0.41,"sign":-1,"group":"K11: Digestive system diseases","label":"Other diseases of intestine","text":"Phenotype: Other diseases of intestine<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.41<br>N cases: 3131<br>N controls: 301931"}
{"pvalue":0.531,"sign":-1,"group":"K11: Digestive system diseases","label":"Other diseases of peritoneum","text":"Phenotype: Other diseases of peritoneum<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.531<br>N cases: 1289<br>N controls: 374197"}
{"pvalue":0.807,"sign":-1,"group":"K11: Digestive system diseases","label":"Overjet","text":"Phenotype: Overjet<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.807<br>N cases: 492<br>N controls: 376785"}
{"pvalue":0.965,"sign":-1,"group":"K11: Digestive system diseases","label":"Other diseases of pancreas","text":"Phenotype: Other diseases of pancreas<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.965<br>N cases: 1791<br>N controls: 330903"}
{"pvalue":0.39,"sign":1,"group":"K11: Digestive system diseases","label":"Paralytic ileus","text":"Phenotype: Paralytic ileus<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.39<br>N cases: 1065<br>N controls: 301931"}
{"pvalue":0.391,"sign":-1,"group":"K11: Digestive system diseases","label":"Parodontitis or/and operation codes","text":"Phenotype: Parodontitis or/and operation codes<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.391<br>N cases: 27833<br>N controls: 349444"}
{"pvalue":0.37,"sign":-1,"group":"K11: Digestive system diseases","label":"Parodontitis or operation codes","text":"Phenotype: Parodontitis or operation codes<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.37<br>N cases: 30377<br>N controls: 346900"}
{"pvalue":0.301,"sign":1,"group":"K11: Digestive system diseases","label":"Chronic periapical parodontitis","text":"Phenotype: Chronic periapical parodontitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.301<br>N cases: 6466<br>N controls: 259234"}
{"pvalue":0.247,"sign":1,"group":"K11: Digestive system diseases","label":"Perforation of oesophagus","text":"Phenotype: Perforation of oesophagus<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.247<br>N cases: 114<br>N controls: 320387"}
{"pvalue":0.184,"sign":-1,"group":"K11: Digestive system diseases","label":"Chronic periodontitis, complicated","text":"Phenotype: Chronic periodontitis, complicated<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.184<br>N cases: 2462<br>N controls: 374815"}
{"pvalue":0.616,"sign":-1,"group":"K11: Digestive system diseases","label":"Chronic periodontitis","text":"Phenotype: Chronic periodontitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.616<br>N cases: 4434<br>N controls: 259234"}
{"pvalue":0.981,"sign":1,"group":"K11: Digestive system diseases","label":"Periodontal disease, other/unspecified","text":"Phenotype: Periodontal disease, other/unspecified<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.981<br>N cases: 92<br>N controls: 289780"}
{"pvalue":0.176,"sign":-1,"group":"K11: Digestive system diseases","label":"Diseases of peritoneum","text":"Phenotype: Diseases of peritoneum<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.176<br>N cases: 3080<br>N controls: 374197"}
{"pvalue":0.173,"sign":-1,"group":"K11: Digestive system diseases","label":"Acute peritonitis","text":"Phenotype: Acute peritonitis<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.173<br>N cases: 1810<br>N controls: 374197"}
{"pvalue":0.338,"sign":1,"group":"K11: Digestive system diseases","label":"Postprocedural disorders of digestive system, not elsewhere classified","text":"Phenotype: Postprocedural disorders of digestive system, not elsewhere classified<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.338<br>N cases: 821<br>N controls: 361055"}
{"pvalue":0.628,"sign":-1,"group":"K11: Digestive system diseases","label":"Colitis, primary sclerosing, strict definition","text":"Phenotype: Colitis, primary sclerosing, strict definition<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.628<br>N cases: 297<br>N controls: 375562"}
{"pvalue":0.189,"sign":-1,"group":"K11: Digestive system diseases","label":"Peptic ulcer","text":"Phenotype: Peptic ulcer<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.189<br>N cases: 264<br>N controls: 320387"}
{"pvalue":0.434,"sign":1,"group":"K11: Digestive system diseases","label":"Dental pulpitis 1, only avohilmo","text":"Phenotype: Dental pulpitis 1, only avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.434<br>N cases: 81713<br>N controls: 295564"}
{"pvalue":0.61,"sign":-1,"group":"K11: Digestive system diseases","label":"Dental pulpitis 3","text":"Phenotype: Dental pulpitis 3<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.61<br>N cases: 4261<br>N controls: 373016"}
{"pvalue":0.0542,"sign":1,"group":"K11: Digestive system diseases","label":"Diseases of pulp and periapical tissues","text":"Phenotype: Diseases of pulp and periapical tissues<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0542<br>N cases: 12078<br>N controls: 259234"}
{"pvalue":0.213,"sign":1,"group":"K11: Digestive system diseases","label":"Pathological resorption of teeth","text":"Phenotype: Pathological resorption of teeth<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.213<br>N cases: 154<br>N controls: 259234"}
{"pvalue":0.0643,"sign":-1,"group":"K11: Digestive system diseases","label":"Maxillary retrognathism , including avohilmo","text":"Phenotype: Maxillary retrognathism , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0643<br>N cases: 443<br>N controls: 376834"}
{"pvalue":0.538,"sign":1,"group":"K11: Digestive system diseases","label":"Diseases of salivary glands","text":"Phenotype: Diseases of salivary glands<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.538<br>N cases: 6269<br>N controls: 259234"}
{"pvalue":0.0238,"sign":-1,"group":"K11: Digestive system diseases","label":"Scissor bite , including avohilmo","text":"Phenotype: Scissor bite , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0238<br>N cases: 518<br>N controls: 376759"}
{"pvalue":0.502,"sign":-1,"group":"K11: Digestive system diseases","label":"Stomatitis and related lesions","text":"Phenotype: Stomatitis and related lesions<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.502<br>N cases: 2459<br>N controls: 259234"}
{"pvalue":0.854,"sign":-1,"group":"K11: Digestive system diseases","label":"Supernumerary teeth EXCLUDE clefts and syndromes","text":"Phenotype: Supernumerary teeth EXCLUDE clefts and syndromes<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.854<br>N cases: 103<br>N controls: 377174"}
{"pvalue":0.109,"sign":-1,"group":"K11: Digestive system diseases","label":"Supernumerary teeth EXCLUDE clefts and syndromes , including avohilmo","text":"Phenotype: Supernumerary teeth EXCLUDE clefts and syndromes , including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.109<br>N cases: 220<br>N controls: 376724"}
{"pvalue":0.994,"sign":1,"group":"K11: Digestive system diseases","label":"Other diseases of hard tissues of teeth","text":"Phenotype: Other diseases of hard tissues of teeth<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.994<br>N cases: 3132<br>N controls: 259234"}
{"pvalue":0.172,"sign":1,"group":"K11: Digestive system diseases","label":"Disease of hard tissues of teeth, NOS","text":"Phenotype: Disease of hard tissues of teeth, NOS<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.172<br>N cases: 125<br>N controls: 259234"}
{"pvalue":0.511,"sign":1,"group":"K11: Digestive system diseases","label":"Disorders of tooth development and eruption","text":"Phenotype: Disorders of tooth development and eruption<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.511<br>N cases: 1579<br>N controls: 259234"}
{"pvalue":0.489,"sign":-1,"group":"K11: Digestive system diseases","label":"Toxic liver disease","text":"Phenotype: Toxic liver disease<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.489<br>N cases: 388<br>N controls: 366450"}
{"pvalue":0.594,"sign":-1,"group":"K11: Digestive system diseases","label":"Ulcerative colitis (strict definition, require KELA, min 2 HDR)","text":"Phenotype: Ulcerative colitis (strict definition, require KELA, min 2 HDR)<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.594<br>N cases: 5034<br>N controls: 371530"}
{"pvalue":0.103,"sign":1,"group":"K11: Digestive system diseases","label":"Umbilical hernia","text":"Phenotype: Umbilical hernia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.103<br>N cases: 8510<br>N controls: 322586"}
{"pvalue":0.572,"sign":1,"group":"K11: Digestive system diseases","label":"Vascular disorders of the intestines","text":"Phenotype: Vascular disorders of the intestines<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.572<br>N cases: 1802<br>N controls: 301931"}
{"pvalue":0.132,"sign":1,"group":"K11: Digestive system diseases","label":"Ventral hernia","text":"Phenotype: Ventral hernia<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.132<br>N cases: 7628<br>N controls: 322586"}
{"pvalue":0.664,"sign":1,"group":"K11: Digestive system diseases","label":"Volvulus","text":"Phenotype: Volvulus<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.664<br>N cases: 702<br>N controls: 301931"}
{"pvalue":0.871,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Cutaneous abscess, furuncle and carbuncle","text":"Phenotype: Cutaneous abscess, furuncle and carbuncle<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.871<br>N cases: 8157<br>N controls: 355969"}
{"pvalue":0.621,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Acanthosis nigricans","text":"Phenotype: Acanthosis nigricans<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.621<br>N cases: 93<br>N controls: 353088"}
{"pvalue":0.549,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Acne conglobata","text":"Phenotype: Acne conglobata<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.549<br>N cases: 128<br>N controls: 361140"}
{"pvalue":0.0117,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Acne","text":"Phenotype: Acne<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0117<br>N cases: 2787<br>N controls: 361140"}
{"pvalue":0.795,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other  and unspecified acne","text":"Phenotype: Other  and unspecified acne<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.795<br>N cases: 335<br>N controls: 361140"}
{"pvalue":0.327,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Acquired keratosis [keratoderma] palmaris et plantaris","text":"Phenotype: Acquired keratosis [keratoderma] palmaris et plantaris<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.327<br>N cases: 115<br>N controls: 353088"}
{"pvalue":0.0471,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Actinic keratosis","text":"Phenotype: Actinic keratosis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0471<br>N cases: 11081<br>N controls: 364831"}
{"pvalue":0.0373,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Allergic contact dermatitis","text":"Phenotype: Allergic contact dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0373<br>N cases: 4336<br>N controls: 336589"}
{"pvalue":0.505,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Androgenic alopecia","text":"Phenotype: Androgenic alopecia<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.505<br>N cases: 195<br>N controls: 201019"}
{"pvalue":0.433,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Alopecia areata","text":"Phenotype: Alopecia areata<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.433<br>N cases: 682<br>N controls: 361140"}
{"pvalue":0.479,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Apocrine sweat disorders, other sweat gland disorders","text":"Phenotype: Apocrine sweat disorders, other sweat gland disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.479<br>N cases: 106<br>N controls: 361140"}
{"pvalue":1.36e-07,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Atopic dermatitis","text":"Phenotype: Atopic dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 1.36e-07<br>N cases: 13473<br>N controls: 336589"}
{"pvalue":0.559,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Atrophic disorders of skin","text":"Phenotype: Atrophic disorders of skin<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.559<br>N cases: 3839<br>N controls: 353088"}
{"pvalue":0.0832,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified atrophic disorders of skin","text":"Phenotype: Other and unspecified atrophic disorders of skin<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0832<br>N cases: 115<br>N controls: 353088"}
{"pvalue":0.209,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other bullous disorders","text":"Phenotype: Other bullous disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.209<br>N cases: 710<br>N controls: 375767"}
{"pvalue":0.326,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Bullous disorders","text":"Phenotype: Bullous disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.326<br>N cases: 1510<br>N controls: 375767"}
{"pvalue":0.168,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Cellulitis","text":"Phenotype: Cellulitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.168<br>N cases: 6683<br>N controls: 355969"}
{"pvalue":0.897,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Chloasma","text":"Phenotype: Chloasma<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.897<br>N cases: 95<br>N controls: 353088"}
{"pvalue":0.581,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Chronic ulcer of skin, not elsewhere classified","text":"Phenotype: Chronic ulcer of skin, not elsewhere classified<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.581<br>N cases: 1840<br>N controls: 353088"}
{"pvalue":0.103,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Corns and callosities","text":"Phenotype: Corns and callosities<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.103<br>N cases: 1978<br>N controls: 353088"}
{"pvalue":0.0634,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Cutis laxa senilis","text":"Phenotype: Cutis laxa senilis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0634<br>N cases: 184<br>N controls: 364831"}
{"pvalue":0.88,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Decubitus ulcer and pressure area","text":"Phenotype: Decubitus ulcer and pressure area<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.88<br>N cases: 1479<br>N controls: 353088"}
{"pvalue":0.107,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Dermatitis herpetiformis","text":"Phenotype: Dermatitis herpetiformis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.107<br>N cases: 483<br>N controls: 375767"}
{"pvalue":0.00011,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Dermatitis and eczema","text":"Phenotype: Dermatitis and eczema<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.000107<br>N cases: 40688<br>N controls: 336589"}
{"pvalue":0.119,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified dermatitis","text":"Phenotype: Other and unspecified dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.119<br>N cases: 21951<br>N controls: 336589"}
{"pvalue":0.312,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Nummular dermatitis","text":"Phenotype: Nummular dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.312<br>N cases: 2164<br>N controls: 336589"}
{"pvalue":0.3,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Disorders of skin appendages","text":"Phenotype: Disorders of skin appendages<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.3<br>N cases: 16137<br>N controls: 361140"}
{"pvalue":0.762,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Dyshidrosis [pompholyx]","text":"Phenotype: Dyshidrosis [pompholyx]<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.762<br>N cases: 405<br>N controls: 336589"}
{"pvalue":0.816,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other epidermal thickening","text":"Phenotype: Other epidermal thickening<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.816<br>N cases: 1112<br>N controls: 353088"}
{"pvalue":0.646,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified epidermal thickening","text":"Phenotype: Other and unspecified epidermal thickening<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.646<br>N cases: 685<br>N controls: 353088"}
{"pvalue":0.58,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Erythema multiforme","text":"Phenotype: Erythema multiforme<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.58<br>N cases: 612<br>N controls: 364583"}
{"pvalue":0.47,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Erythema nodosum","text":"Phenotype: Erythema nodosum<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.47<br>N cases: 814<br>N controls: 364583"}
{"pvalue":0.966,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other erythematous conditions","text":"Phenotype: Other erythematous conditions<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.966<br>N cases: 878<br>N controls: 364583"}
{"pvalue":0.919,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Universal erythroderma, KELA reimbursement","text":"Phenotype: Universal erythroderma, KELA reimbursement<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.919<br>N cases: 389<br>N controls: 364583"}
{"pvalue":0.843,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Erythema intertrigo","text":"Phenotype: Erythema intertrigo<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.843<br>N cases: 570<br>N controls: 336589"}
{"pvalue":0.324,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Exfoliative dermatitis","text":"Phenotype: Exfoliative dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.324<br>N cases: 298<br>N controls: 336589"}
{"pvalue":0.631,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Factitial dermatitis","text":"Phenotype: Factitial dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.631<br>N cases: 135<br>N controls: 353088"}
{"pvalue":0.24,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other follicular disorders","text":"Phenotype: Other follicular disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.24<br>N cases: 1918<br>N controls: 361140"}
{"pvalue":0.609,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Follicular cysts of skin and subcutaneous tissue","text":"Phenotype: Follicular cysts of skin and subcutaneous tissue<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.609<br>N cases: 5459<br>N controls: 361140"}
{"pvalue":0.0268,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified follicular disorders","text":"Phenotype: Other and unspecified follicular disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0268<br>N cases: 971<br>N controls: 361140"}
{"pvalue":0.174,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Dermatitis due to ingested food","text":"Phenotype: Dermatitis due to ingested food<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.174<br>N cases: 955<br>N controls: 336589"}
{"pvalue":0.634,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Foreign body granuloma of skin and subcutaneous tissue","text":"Phenotype: Foreign body granuloma of skin and subcutaneous tissue<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.634<br>N cases: 87<br>N controls: 353088"}
{"pvalue":0.914,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Granuloma annulare","text":"Phenotype: Granuloma annulare<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.914<br>N cases: 354<br>N controls: 353088"}
{"pvalue":0.178,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified granulomatous disorders of skin and subcutaneous tissue","text":"Phenotype: Other and unspecified granulomatous disorders of skin and subcutaneous tissue<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.178<br>N cases: 91<br>N controls: 353088"}
{"pvalue":0.926,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Granulomatous disorders of skin and subcutaneous tissue","text":"Phenotype: Granulomatous disorders of skin and subcutaneous tissue<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.926<br>N cases: 679<br>N controls: 353088"}
{"pvalue":0.355,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Hair colour and hair shaft abnormalities","text":"Phenotype: Hair colour and hair shaft abnormalities<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.355<br>N cases: 113<br>N controls: 361140"}
{"pvalue":0.409,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other nonscarring hair loss","text":"Phenotype: Other nonscarring hair loss<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.409<br>N cases: 198<br>N controls: 361140"}
{"pvalue":0.8,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified nonscarring hair loss","text":"Phenotype: Other and unspecified nonscarring hair loss<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.8<br>N cases: 147<br>N controls: 361140"}
{"pvalue":0.801,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Cicatricial alopecia [scarring hair loss]","text":"Phenotype: Cicatricial alopecia [scarring hair loss]<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.801<br>N cases: 187<br>N controls: 361140"}
{"pvalue":0.449,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Hidradenitis suppurativa","text":"Phenotype: Hidradenitis suppurativa<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.449<br>N cases: 931<br>N controls: 361140"}
{"pvalue":0.0637,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Hirsutism in women","text":"Phenotype: Hirsutism in women<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0637<br>N cases: 458<br>N controls: 201019"}
{"pvalue":0.366,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other hypertrichosis","text":"Phenotype: Other hypertrichosis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.366<br>N cases: 82<br>N controls: 361140"}
{"pvalue":0.524,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified hypertrophic disorders of skin","text":"Phenotype: Other and unspecified hypertrophic disorders of skin<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.524<br>N cases: 143<br>N controls: 353088"}
{"pvalue":0.939,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Hypertrophic scar","text":"Phenotype: Hypertrophic scar<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.939<br>N cases: 1476<br>N controls: 353088"}
{"pvalue":0.171,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Impetigo","text":"Phenotype: Impetigo<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.171<br>N cases: 1215<br>N controls: 355969"}
{"pvalue":0.252,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Infective dermatitis","text":"Phenotype: Infective dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.252<br>N cases: 3405<br>N controls: 336589"}
{"pvalue":0.0365,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Infections of the skin and subcutaneous tissue","text":"Phenotype: Infections of the skin and subcutaneous tissue<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0365<br>N cases: 21308<br>N controls: 355969"}
{"pvalue":0.162,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other local infections of skin and subcutaneous tissue","text":"Phenotype: Other local infections of skin and subcutaneous tissue<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.162<br>N cases: 2801<br>N controls: 355969"}
{"pvalue":0.663,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Dermatitis due to substances taken internally","text":"Phenotype: Dermatitis due to substances taken internally<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.663<br>N cases: 2469<br>N controls: 336589"}
{"pvalue":0.726,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Lichen planus","text":"Phenotype: Lichen planus<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.726<br>N cases: 3597<br>N controls: 364071"}
{"pvalue":0.486,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Lichen planus, including avohilmo","text":"Phenotype: Lichen planus, including avohilmo<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.486<br>N cases: 5015<br>N controls: 372262"}
{"pvalue":0.571,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Lichen sclerosus et atrophicus","text":"Phenotype: Lichen sclerosus et atrophicus<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.571<br>N cases: 2445<br>N controls: 353088"}
{"pvalue":0.333,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Lichen simplex chronicus","text":"Phenotype: Lichen simplex chronicus<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.333<br>N cases: 901<br>N controls: 336589"}
{"pvalue":0.51,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Lichen simplex chronicus and prurigo","text":"Phenotype: Lichen simplex chronicus and prurigo<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.51<br>N cases: 1703<br>N controls: 336589"}
{"pvalue":0.116,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Livedoid vasculitis","text":"Phenotype: Livedoid vasculitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.116<br>N cases: 86<br>N controls: 353088"}
{"pvalue":0.868,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified localized connective tissue disorders","text":"Phenotype: Other and unspecified localized connective tissue disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.868<br>N cases: 82<br>N controls: 353088"}
{"pvalue":0.904,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other localized connective tissue disorders","text":"Phenotype: Other localized connective tissue disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.904<br>N cases: 493<br>N controls: 353088"}
{"pvalue":0.643,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Localized scleroderma [morphea]","text":"Phenotype: Localized scleroderma [morphea]<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.643<br>N cases: 361<br>N controls: 353088"}
{"pvalue":0.688,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Lupus erythematosus","text":"Phenotype: Lupus erythematosus<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.688<br>N cases: 652<br>N controls: 353088"}
{"pvalue":0.11,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Acute lymphadenitis","text":"Phenotype: Acute lymphadenitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.11<br>N cases: 1812<br>N controls: 355969"}
{"pvalue":0.706,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Nail disorders","text":"Phenotype: Nail disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.706<br>N cases: 2254<br>N controls: 361140"}
{"pvalue":0.461,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Nail dystrophy","text":"Phenotype: Nail dystrophy<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.461<br>N cases: 167<br>N controls: 361140"}
{"pvalue":0.372,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Ingrowing nail","text":"Phenotype: Ingrowing nail<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.372<br>N cases: 1477<br>N controls: 361140"}
{"pvalue":0.603,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Onycholysis","text":"Phenotype: Onycholysis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.603<br>N cases: 153<br>N controls: 361140"}
{"pvalue":0.605,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified nail disorders","text":"Phenotype: Other and unspecified nail disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.605<br>N cases: 453<br>N controls: 361140"}
{"pvalue":0.877,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Necrobiosis lipoidica, not elsewhere classified","text":"Phenotype: Necrobiosis lipoidica, not elsewhere classified<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.877<br>N cases: 161<br>N controls: 353088"}
{"pvalue":0.592,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified skin changes due to chronic exposure to nonionizing radiation","text":"Phenotype: Other and unspecified skin changes due to chronic exposure to nonionizing radiation<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.592<br>N cases: 353<br>N controls: 364831"}
{"pvalue":0.891,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other acute skin changes due to ultraviolet radiation","text":"Phenotype: Other acute skin changes due to ultraviolet radiation<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.891<br>N cases: 996<br>N controls: 364831"}
{"pvalue":0.917,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified acute skin changes due to ultraviolet radiation","text":"Phenotype: Other and unspecified acute skin changes due to ultraviolet radiation<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.917<br>N cases: 732<br>N controls: 364831"}
{"pvalue":0.811,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified bullous disorders","text":"Phenotype: Other and unspecified bullous disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.811<br>N cases: 242<br>N controls: 375767"}
{"pvalue":0.0208,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other contact dermatitis","text":"Phenotype: Other contact dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0208<br>N cases: 2490<br>N controls: 336589"}
{"pvalue":0.614,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other disorders of skin and subcutaneous tissue, not elsewhere classified","text":"Phenotype: Other disorders of skin and subcutaneous tissue, not elsewhere classified<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.614<br>N cases: 4387<br>N controls: 353088"}
{"pvalue":0.682,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other infiltrative disorders of skin and subcutaneous tissue","text":"Phenotype: Other infiltrative disorders of skin and subcutaneous tissue<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.682<br>N cases: 120<br>N controls: 353088"}
{"pvalue":0.0538,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other melanin hyperpigmentation","text":"Phenotype: Other melanin hyperpigmentation<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0538<br>N cases: 510<br>N controls: 353088"}
{"pvalue":0.748,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other disorders of skin and subcutaneous tissue","text":"Phenotype: Other disorders of skin and subcutaneous tissue<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.748<br>N cases: 24189<br>N controls: 353088"}
{"pvalue":0.173,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other disorders of pigmentation","text":"Phenotype: Other disorders of pigmentation<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.173<br>N cases: 1080<br>N controls: 353088"}
{"pvalue":0.00984,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Papulosquamous disorders","text":"Phenotype: Papulosquamous disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00984<br>N cases: 13206<br>N controls: 364071"}
{"pvalue":0.158,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other papulosquamous disorders","text":"Phenotype: Other papulosquamous disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.158<br>N cases: 263<br>N controls: 364071"}
{"pvalue":0.269,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified papulosquamous disorders","text":"Phenotype: Other and unspecified papulosquamous disorders<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.269<br>N cases: 139<br>N controls: 364071"}
{"pvalue":0.512,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pityriasis lichenoides chronica","text":"Phenotype: Pityriasis lichenoides chronica<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.512<br>N cases: 103<br>N controls: 364071"}
{"pvalue":0.661,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified parapsoriasis","text":"Phenotype: Other and unspecified parapsoriasis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.661<br>N cases: 113<br>N controls: 364071"}
{"pvalue":0.764,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Parapsoriasis","text":"Phenotype: Parapsoriasis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.764<br>N cases: 488<br>N controls: 364071"}
{"pvalue":0.935,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Bullous pemphigoid","text":"Phenotype: Bullous pemphigoid<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.935<br>N cases: 507<br>N controls: 375767"}
{"pvalue":0.491,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified pemphigoid","text":"Phenotype: Other and unspecified pemphigoid<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.491<br>N cases: 186<br>N controls: 375767"}
{"pvalue":0.448,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pemphigus","text":"Phenotype: Pemphigus<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.448<br>N cases: 162<br>N controls: 375767"}
{"pvalue":0.76,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Perioral dermatitis","text":"Phenotype: Perioral dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.76<br>N cases: 465<br>N controls: 361140"}
{"pvalue":0.543,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified disorders of pigmentation","text":"Phenotype: Other and unspecified disorders of pigmentation<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.543<br>N cases: 181<br>N controls: 353088"}
{"pvalue":0.863,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pigmented purpuric dermatosis","text":"Phenotype: Pigmented purpuric dermatosis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.863<br>N cases: 230<br>N controls: 353088"}
{"pvalue":0.835,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pilonidal cyst","text":"Phenotype: Pilonidal cyst<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.835<br>N cases: 2739<br>N controls: 355969"}
{"pvalue":0.535,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pityriasis rosea","text":"Phenotype: Pityriasis rosea<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.535<br>N cases: 182<br>N controls: 364071"}
{"pvalue":0.441,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Polymorphous light eruption","text":"Phenotype: Polymorphous light eruption<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.441<br>N cases: 194<br>N controls: 364831"}
{"pvalue":0.538,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other  prurigo","text":"Phenotype: Other  prurigo<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.538<br>N cases: 283<br>N controls: 336589"}
{"pvalue":0.266,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Prurigo nodularis","text":"Phenotype: Prurigo nodularis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.266<br>N cases: 606<br>N controls: 336589"}
{"pvalue":0.586,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pruritus","text":"Phenotype: Pruritus<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.586<br>N cases: 2994<br>N controls: 336589"}
{"pvalue":0.00088,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Psoriasis","text":"Phenotype: Psoriasis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.000876<br>N cases: 9267<br>N controls: 364071"}
{"pvalue":0.904,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Guttate psoriasis","text":"Phenotype: Guttate psoriasis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.904<br>N cases: 343<br>N controls: 364071"}
{"pvalue":0.0233,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified psoriasis","text":"Phenotype: Other and unspecified psoriasis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0233<br>N cases: 1667<br>N controls: 364071"}
{"pvalue":0.188,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Generalized pustular psoriasis","text":"Phenotype: Generalized pustular psoriasis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.188<br>N cases: 89<br>N controls: 364071"}
{"pvalue":0.191,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pustulosis palmaris et plantaris","text":"Phenotype: Pustulosis palmaris et plantaris<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.191<br>N cases: 1112<br>N controls: 364071"}
{"pvalue":0.024,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Psoriasis vulgaris","text":"Phenotype: Psoriasis vulgaris<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.024<br>N cases: 5759<br>N controls: 364071"}
{"pvalue":0.966,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pyoderma gangrenosum","text":"Phenotype: Pyoderma gangrenosum<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.966<br>N cases: 154<br>N controls: 353088"}
{"pvalue":0.0753,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pyoderma","text":"Phenotype: Pyoderma<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0753<br>N cases: 537<br>N controls: 355969"}
{"pvalue":0.849,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Pyogenic granuloma","text":"Phenotype: Pyogenic granuloma<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.849<br>N cases: 412<br>N controls: 353088"}
{"pvalue":0.679,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Rhinophyma","text":"Phenotype: Rhinophyma<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.679<br>N cases: 135<br>N controls: 361140"}
{"pvalue":0.349,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified rosacea","text":"Phenotype: Other and unspecified rosacea<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.349<br>N cases: 2210<br>N controls: 361140"}
{"pvalue":0.647,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Scar conditions and fibrosis of skin","text":"Phenotype: Scar conditions and fibrosis of skin<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.647<br>N cases: 1027<br>N controls: 353088"}
{"pvalue":0.989,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Seborrhoeic dermatitis","text":"Phenotype: Seborrhoeic dermatitis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.989<br>N cases: 2688<br>N controls: 336589"}
{"pvalue":0.627,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Seborrhoeic keratosis","text":"Phenotype: Seborrhoeic keratosis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.627<br>N cases: 5835<br>N controls: 353088"}
{"pvalue":0.878,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified disorders of skin and subcutaneous tissue","text":"Phenotype: Other and unspecified disorders of skin and subcutaneous tissue<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.878<br>N cases: 1950<br>N controls: 353088"}
{"pvalue":0.909,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Striae atrophicae","text":"Phenotype: Striae atrophicae<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.909<br>N cases: 281<br>N controls: 353088"}
{"pvalue":0.475,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Ulcer of lower limb, not elsewhere classified","text":"Phenotype: Ulcer of lower limb, not elsewhere classified<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.475<br>N cases: 3784<br>N controls: 353088"}
{"pvalue":0.304,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Allergic urticaria","text":"Phenotype: Allergic urticaria<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.304<br>N cases: 2386<br>N controls: 364583"}
{"pvalue":0.88,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Cholinergic urticaria","text":"Phenotype: Cholinergic urticaria<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.88<br>N cases: 130<br>N controls: 364583"}
{"pvalue":0.178,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Urticaria due to cold and heat","text":"Phenotype: Urticaria due to cold and heat<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.178<br>N cases: 209<br>N controls: 364583"}
{"pvalue":0.034,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Dermatographic urticaria","text":"Phenotype: Dermatographic urticaria<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.034<br>N cases: 1848<br>N controls: 364583"}
{"pvalue":0.83,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Idiopathic urticaria","text":"Phenotype: Idiopathic urticaria<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.83<br>N cases: 518<br>N controls: 364583"}
{"pvalue":0.114,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified urticaria","text":"Phenotype: Other and unspecified urticaria<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.114<br>N cases: 6381<br>N controls: 364583"}
{"pvalue":0.0194,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Urticaria","text":"Phenotype: Urticaria<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0194<br>N cases: 10175<br>N controls: 364583"}
{"pvalue":0.118,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Other and unspecified vasculitis limited to skin","text":"Phenotype: Other and unspecified vasculitis limited to skin<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.118<br>N cases: 600<br>N controls: 353088"}
{"pvalue":0.435,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Vitiligo","text":"Phenotype: Vitiligo<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.435<br>N cases: 260<br>N controls: 353088"}
{"pvalue":0.694,"sign":1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Xerosis cutis","text":"Phenotype: Xerosis cutis<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.694<br>N cases: 326<br>N controls: 353088"}
{"pvalue":0.885,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Localized skin eruption due to drugs and medicaments","text":"Phenotype: Localized skin eruption due to drugs and medicaments<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.885<br>N cases: 272<br>N controls: 377005"}
{"pvalue":0.968,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Abscess of tendon sheath","text":"Phenotype: Abscess of tendon sheath<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.968<br>N cases: 145<br>N controls: 275212"}
{"pvalue":0.72,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Achilles tendinitis","text":"Phenotype: Achilles tendinitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.72<br>N cases: 3113<br>N controls: 270964"}
{"pvalue":0.116,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Adhesive capsulitis of shoulder","text":"Phenotype: Adhesive capsulitis of shoulder<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.116<br>N cases: 5538<br>N controls: 275212"}
{"pvalue":0.772,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Algoneurodystrophy","text":"Phenotype: Algoneurodystrophy<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.772<br>N cases: 888<br>N controls: 358014"}
{"pvalue":0.592,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other acquired deformities of ankle and foot","text":"Phenotype: Other acquired deformities of ankle and foot<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.592<br>N cases: 207<br>N controls: 240862"}
{"pvalue":0.235,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Ankylosis of joint","text":"Phenotype: Ankylosis of joint<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.235<br>N cases: 153<br>N controls: 240862"}
{"pvalue":0.00018,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Ankylosing spondylitis","text":"Phenotype: Ankylosing spondylitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.000183<br>N cases: 2860<br>N controls: 270964"}
{"pvalue":0.00466,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Ankylosing spondylitis, strict definition","text":"Phenotype: Ankylosing spondylitis, strict definition<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00466<br>N cases: 1193<br>N controls: 374621"}
{"pvalue":0.0228,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Arthropathies in other diseases classified elsewhere","text":"Phenotype: Arthropathies in other diseases classified elsewhere<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0228<br>N cases: 1060<br>N controls: 240862"}
{"pvalue":0.512,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Arthropathies","text":"Phenotype: Arthropathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.512<br>N cases: 136415<br>N controls: 240862"}
{"pvalue":0.353,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Arthrosis","text":"Phenotype: Arthrosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.353<br>N cases: 73710<br>N controls: 240862"}
{"pvalue":0.285,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Artrosis, including avohilmo","text":"Phenotype: Artrosis, including avohilmo<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.285<br>N cases: 96500<br>N controls: 280777"}
{"pvalue":0.34,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Gonarthrosis","text":"Phenotype: Gonarthrosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.34<br>N cases: 44688<br>N controls: 240862"}
{"pvalue":0.398,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Gonarthrosis, primary, with knee surgery","text":"Phenotype: Gonarthrosis, primary, with knee surgery<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.398<br>N cases: 19126<br>N controls: 337196"}
{"pvalue":0.743,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other arthrosis","text":"Phenotype: Other arthrosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.743<br>N cases: 20949<br>N controls: 240862"}
{"pvalue":0.0665,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Polyarthrosis","text":"Phenotype: Polyarthrosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0665<br>N cases: 6185<br>N controls: 240862"}
{"pvalue":0.189,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Coxarthrosis,","text":"Phenotype: Coxarthrosis,<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.189<br>N cases: 22254<br>N controls: 240862"}
{"pvalue":0.142,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Coxarthrosis, primary, with hip surgery","text":"Phenotype: Coxarthrosis, primary, with hip surgery<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.142<br>N cases: 14990<br>N controls: 357221"}
{"pvalue":0.134,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Coxarthrosis, primary","text":"Phenotype: Coxarthrosis, primary<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.134<br>N cases: 20056<br>N controls: 357221"}
{"pvalue":0.0723,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Atlantoaxial subluxation","text":"Phenotype: Atlantoaxial subluxation<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0723<br>N cases: 176<br>N controls: 270964"}
{"pvalue":0.0825,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Synovial cyst of popliteal space [Baker]","text":"Phenotype: Synovial cyst of popliteal space [Baker]<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0825<br>N cases: 2084<br>N controls: 275212"}
{"pvalue":0.758,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Behçet disease","text":"Phenotype: Behçet disease<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.758<br>N cases: 85<br>N controls: 365533"}
{"pvalue":0.682,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Bicipital tendinitis","text":"Phenotype: Bicipital tendinitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.682<br>N cases: 1317<br>N controls: 275212"}
{"pvalue":0.261,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Biomechanical lesions, not elsewhere classified","text":"Phenotype: Biomechanical lesions, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.261<br>N cases: 1105<br>N controls: 373303"}
{"pvalue":0.714,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Disorders of continuity of bone","text":"Phenotype: Disorders of continuity of bone<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.714<br>N cases: 2543<br>N controls: 358014"}
{"pvalue":0.0488,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other disorders of bone density and structure","text":"Phenotype: Other disorders of bone density and structure<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0488<br>N cases: 677<br>N controls: 358014"}
{"pvalue":0.907,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other specified/unspecified disorders of  bone/cartilage","text":"Phenotype: Other specified/unspecified disorders of  bone/cartilage<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.907<br>N cases: 769<br>N controls: 358014"}
{"pvalue":0.474,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Hypertrophy of bone","text":"Phenotype: Hypertrophy of bone<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.474<br>N cases: 84<br>N controls: 358014"}
{"pvalue":0.308,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other bursal cyst","text":"Phenotype: Other bursal cyst<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.308<br>N cases: 393<br>N controls: 275212"}
{"pvalue":0.608,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other bursitis of elbow","text":"Phenotype: Other bursitis of elbow<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.608<br>N cases: 169<br>N controls: 275212"}
{"pvalue":0.85,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other bursitis of hip","text":"Phenotype: Other bursitis of hip<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.85<br>N cases: 492<br>N controls: 275212"}
{"pvalue":0.716,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other bursitis of knee","text":"Phenotype: Other bursitis of knee<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.716<br>N cases: 347<br>N controls: 275212"}
{"pvalue":0.0328,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other bursitis, not elsewhere classified","text":"Phenotype: Other bursitis, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0328<br>N cases: 282<br>N controls: 275212"}
{"pvalue":0.669,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other bursopathies","text":"Phenotype: Other bursopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.669<br>N cases: 3988<br>N controls: 275212"}
{"pvalue":0.86,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Calcaneal spur","text":"Phenotype: Calcaneal spur<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.86<br>N cases: 300<br>N controls: 275212"}
{"pvalue":0.999,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Calcific tendinitis of shoulder","text":"Phenotype: Calcific tendinitis of shoulder<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.999<br>N cases: 1646<br>N controls: 275212"}
{"pvalue":0.467,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Calcific tendinitis","text":"Phenotype: Calcific tendinitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.467<br>N cases: 240<br>N controls: 275212"}
{"pvalue":0.904,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other articular cartilage disorders","text":"Phenotype: Other articular cartilage disorders<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.904<br>N cases: 723<br>N controls: 240862"}
{"pvalue":0.672,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Cervicalgia","text":"Phenotype: Cervicalgia<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.672<br>N cases: 6684<br>N controls: 270964"}
{"pvalue":0.137,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Cervical disc disorders","text":"Phenotype: Cervical disc disorders<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.137<br>N cases: 13394<br>N controls: 270964"}
{"pvalue":0.358,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Cervicobrachial syndrome","text":"Phenotype: Cervicobrachial syndrome<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.358<br>N cases: 7353<br>N controls: 270964"}
{"pvalue":0.857,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Cervicocranial syndrome","text":"Phenotype: Cervicocranial syndrome<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.857<br>N cases: 3149<br>N controls: 270964"}
{"pvalue":0.964,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Chondromalacia","text":"Phenotype: Chondromalacia<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.964<br>N cases: 794<br>N controls: 370709"}
{"pvalue":0.858,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Chondropathies","text":"Phenotype: Chondropathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.858<br>N cases: 4850<br>N controls: 370709"}
{"pvalue":0.689,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Chronic crepitant synovitis/bursitis of hand and wrist/periarthritis of wrist","text":"Phenotype: Chronic crepitant synovitis/bursitis of hand and wrist/periarthritis of wrist<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.689<br>N cases: 385<br>N controls: 275212"}
{"pvalue":0.699,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Polyarteritis with lung involvement [Churg-Strauss]/EGPA","text":"Phenotype: Polyarteritis with lung involvement [Churg-Strauss]/EGPA<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.699<br>N cases: 99<br>N controls: 365533"}
{"pvalue":0.25,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Acquired clawhand, clubhand, clawfoot and clubfoot","text":"Phenotype: Acquired clawhand, clubhand, clawfoot and clubfoot<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.25<br>N cases: 131<br>N controls: 240862"}
{"pvalue":0.422,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other specified/unspecified systemic involvement of connective tissue","text":"Phenotype: Other specified/unspecified systemic involvement of connective tissue<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.422<br>N cases: 1676<br>N controls: 365533"}
{"pvalue":0.632,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Contracture of joint","text":"Phenotype: Contracture of joint<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.632<br>N cases: 329<br>N controls: 240862"}
{"pvalue":0.515,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other crystal arthropathies","text":"Phenotype: Other crystal arthropathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.515<br>N cases: 444<br>N controls: 240862"}
{"pvalue":0.171,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other acquired deformities of musculoskeletal system and connective tissue","text":"Phenotype: Other acquired deformities of musculoskeletal system and connective tissue<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.171<br>N cases: 1249<br>N controls: 373303"}
{"pvalue":0.814,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Deforming dorsopathies","text":"Phenotype: Deforming dorsopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.814<br>N cases: 9672<br>N controls: 270964"}
{"pvalue":0.0858,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other specified/unspecified deforming dorsopathies","text":"Phenotype: Other specified/unspecified deforming dorsopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0858<br>N cases: 530<br>N controls: 270964"}
{"pvalue":0.811,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Radial styloid tenosynovitis [de Quervain]","text":"Phenotype: Radial styloid tenosynovitis [de Quervain]<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.811<br>N cases: 1552<br>N controls: 275212"}
{"pvalue":0.353,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other dermatomyositis","text":"Phenotype: Other dermatomyositis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.353<br>N cases: 143<br>N controls: 365533"}
{"pvalue":0.543,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Dermatopolymyositis, unspecified","text":"Phenotype: Dermatopolymyositis, unspecified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.543<br>N cases: 147<br>N controls: 365533"}
{"pvalue":0.874,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Diastasis of muscle","text":"Phenotype: Diastasis of muscle<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.874<br>N cases: 162<br>N controls: 275212"}
{"pvalue":0.0361,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Infection of intervertebral disc (pyogenic)","text":"Phenotype: Infection of intervertebral disc (pyogenic)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0361<br>N cases: 296<br>N controls: 270964"}
{"pvalue":0.919,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Discitis, unspecified","text":"Phenotype: Discitis, unspecified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.919<br>N cases: 422<br>N controls: 270964"}
{"pvalue":0.171,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other specified/unspecified disorders of synovium and tendon +Other specified/unspecified bursopathies","text":"Phenotype: Other specified/unspecified disorders of synovium and tendon +Other specified/unspecified bursopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.171<br>N cases: 1354<br>N controls: 275212"}
{"pvalue":0.514,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Dorsalgia","text":"Phenotype: Dorsalgia<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.514<br>N cases: 59438<br>N controls: 270964"}
{"pvalue":0.308,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other/unspecified dorsalgia","text":"Phenotype: Other/unspecified dorsalgia<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.308<br>N cases: 14075<br>N controls: 270964"}
{"pvalue":0.286,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Dorsopathies","text":"Phenotype: Dorsopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.286<br>N cases: 106313<br>N controls: 270964"}
{"pvalue":0.764,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other specified/unspecified dorsopathies","text":"Phenotype: Other specified/unspecified dorsopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.764<br>N cases: 996<br>N controls: 270964"}
{"pvalue":0.554,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other dorsopathies, not elsewhere classified","text":"Phenotype: Other dorsopathies, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.554<br>N cases: 79212<br>N controls: 270964"}
{"pvalue":0.855,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Palmar fascial fibromatosis [Dupuytren]","text":"Phenotype: Palmar fascial fibromatosis [Dupuytren]<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.855<br>N cases: 5128<br>N controls: 275212"}
{"pvalue":0.367,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Early lumbar disc prolapse, operated","text":"Phenotype: Early lumbar disc prolapse, operated<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.367<br>N cases: 8351<br>N controls: 368926"}
{"pvalue":0.291,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Enteropathic arthropathies","text":"Phenotype: Enteropathic arthropathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.291<br>N cases: 655<br>N controls: 240862"}
{"pvalue":0.363,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Enthesopathies of lower limb, excluding foot","text":"Phenotype: Enthesopathies of lower limb, excluding foot<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.363<br>N cases: 7125<br>N controls: 270964"}
{"pvalue":0.0264,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other/unspecified enthesopathies of lower limb, excluding foot","text":"Phenotype: Other/unspecified enthesopathies of lower limb, excluding foot<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0264<br>N cases: 2066<br>N controls: 270964"}
{"pvalue":0.849,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other/unspecified enthesopathies, not elsewhere classified","text":"Phenotype: Other/unspecified enthesopathies, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.849<br>N cases: 2763<br>N controls: 275212"}
{"pvalue":0.662,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other enthesopathies","text":"Phenotype: Other enthesopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.662<br>N cases: 10581<br>N controls: 275212"}
{"pvalue":0.955,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Fatigue fracture of vertebra","text":"Phenotype: Fatigue fracture of vertebra<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.955<br>N cases: 106<br>N controls: 270964"}
{"pvalue":0.952,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Hypertrophy of (infrapatellar) fat pad","text":"Phenotype: Hypertrophy of (infrapatellar) fat pad<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.952<br>N cases: 294<br>N controls: 275212"}
{"pvalue":0.959,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Fibroblastic disorders","text":"Phenotype: Fibroblastic disorders<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.959<br>N cases: 7952<br>N controls: 275212"}
{"pvalue":0.35,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other fibroblastic disorders","text":"Phenotype: Other fibroblastic disorders<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.35<br>N cases: 109<br>N controls: 275212"}
{"pvalue":0.328,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Fibromyalgia","text":"Phenotype: Fibromyalgia<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.328<br>N cases: 2314<br>N controls: 275212"}
{"pvalue":0.38,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Deformity of finger(s)","text":"Phenotype: Deformity of finger(s)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.38<br>N cases: 162<br>N controls: 240862"}
{"pvalue":0.845,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Flat foot [pes planus] (acquired)","text":"Phenotype: Flat foot [pes planus] (acquired)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.845<br>N cases: 2677<br>N controls: 240862"}
{"pvalue":0.527,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Residual foreign body in soft tissue","text":"Phenotype: Residual foreign body in soft tissue<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.527<br>N cases: 1368<br>N controls: 275212"}
{"pvalue":0.46,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Ankylosing hyperostosis [Forestier]","text":"Phenotype: Ankylosing hyperostosis [Forestier]<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.46<br>N cases: 354<br>N controls: 270964"}
{"pvalue":0.116,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Ganglion","text":"Phenotype: Ganglion<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.116<br>N cases: 7270<br>N controls: 275212"}
{"pvalue":0.358,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Giant cell arteritis","text":"Phenotype: Giant cell arteritis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.358<br>N cases: 996<br>N controls: 365533"}
{"pvalue":0.125,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Gluteal tendinitis","text":"Phenotype: Gluteal tendinitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.125<br>N cases: 854<br>N controls: 270964"}
{"pvalue":0.0578,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Gout","text":"Phenotype: Gout<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0578<br>N cases: 8489<br>N controls: 240862"}
{"pvalue":0.867,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other deformity of hallux (acquired)","text":"Phenotype: Other deformity of hallux (acquired)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.867<br>N cases: 223<br>N controls: 240862"}
{"pvalue":0.383,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Hallux rigidus","text":"Phenotype: Hallux rigidus<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.383<br>N cases: 4459<br>N controls: 240862"}
{"pvalue":0.614,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Hallux valgus (acquired)","text":"Phenotype: Hallux valgus (acquired)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.614<br>N cases: 14726<br>N controls: 240862"}
{"pvalue":0.744,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other hammer toe(s) (acquired)","text":"Phenotype: Other hammer toe(s) (acquired)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.744<br>N cases: 5625<br>N controls: 240862"}
{"pvalue":0.434,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Thrombotic microangiopathy","text":"Phenotype: Thrombotic microangiopathy<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.434<br>N cases: 165<br>N controls: 365533"}
{"pvalue":0.492,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Hypersensitivity angiitis","text":"Phenotype: Hypersensitivity angiitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.492<br>N cases: 135<br>N controls: 365533"}
{"pvalue":0.815,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Hypermobility syndrome","text":"Phenotype: Hypermobility syndrome<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.815<br>N cases: 1481<br>N controls: 365533"}
{"pvalue":0.0188,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Iliotibial band syndrome","text":"Phenotype: Iliotibial band syndrome<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0188<br>N cases: 279<br>N controls: 270964"}
{"pvalue":0.789,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Impingement syndrome of shoulder","text":"Phenotype: Impingement syndrome of shoulder<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.789<br>N cases: 8676<br>N controls: 275212"}
{"pvalue":0.523,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Infective bursitis","text":"Phenotype: Infective bursitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.523<br>N cases: 743<br>N controls: 275212"}
{"pvalue":0.488,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other infective (teno)synovitis","text":"Phenotype: Other infective (teno)synovitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.488<br>N cases: 106<br>N controls: 275212"}
{"pvalue":0.116,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other intervertebral disc disorders","text":"Phenotype: Other intervertebral disc disorders<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.116<br>N cases: 37636<br>N controls: 270964"}
{"pvalue":0.46,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Juvenile rheuma","text":"Phenotype: Juvenile rheuma<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.46<br>N cases: 692<br>N controls: 240862"}
{"pvalue":0.929,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Juvenile osteochondrosis","text":"Phenotype: Juvenile osteochondrosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.929<br>N cases: 953<br>N controls: 370709"}
{"pvalue":0.235,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Internal derangement of knee","text":"Phenotype: Internal derangement of knee<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.235<br>N cases: 35511<br>N controls: 240862"}
{"pvalue":0.505,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Kyphosis","text":"Phenotype: Kyphosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.505<br>N cases: 317<br>N controls: 270964"}
{"pvalue":0.136,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Lateral epicondylitis","text":"Phenotype: Lateral epicondylitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.136<br>N cases: 4278<br>N controls: 275212"}
{"pvalue":0.602,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other specified acquired deformities of limbs","text":"Phenotype: Other specified acquired deformities of limbs<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.602<br>N cases: 133<br>N controls: 240862"}
{"pvalue":0.31,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Unequal limb length (acquired)","text":"Phenotype: Unequal limb length (acquired)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.31<br>N cases: 234<br>N controls: 240862"}
{"pvalue":0.962,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Pain in limb","text":"Phenotype: Pain in limb<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.962<br>N cases: 30485<br>N controls: 275212"}
{"pvalue":0.856,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Loose body in joint","text":"Phenotype: Loose body in joint<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.856<br>N cases: 665<br>N controls: 240862"}
{"pvalue":0.604,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Low back pain","text":"Phenotype: Low back pain<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.604<br>N cases: 29329<br>N controls: 270964"}
{"pvalue":0.346,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Lower back pain or/and sciatica","text":"Phenotype: Lower back pain or/and sciatica<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.346<br>N cases: 41815<br>N controls: 335462"}
{"pvalue":0.524,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Mixed connective tissue disease","text":"Phenotype: Mixed connective tissue disease<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.524<br>N cases: 1849<br>N controls: 375428"}
{"pvalue":0.788,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Medial epicondylitis","text":"Phenotype: Medial epicondylitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.788<br>N cases: 1062<br>N controls: 275212"}
{"pvalue":0.023,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Meniscus derangement","text":"Phenotype: Meniscus derangement<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.023<br>N cases: 24158<br>N controls: 240862"}
{"pvalue":0.313,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Metatarsalgia","text":"Phenotype: Metatarsalgia<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.313<br>N cases: 2726<br>N controls: 275212"}
{"pvalue":0.271,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Microscopic polyangiitis","text":"Phenotype: Microscopic polyangiitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.271<br>N cases: 143<br>N controls: 375364"}
{"pvalue":0.755,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Monoarthritis, not elsewhere classified","text":"Phenotype: Monoarthritis, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.755<br>N cases: 1282<br>N controls: 240862"}
{"pvalue":0.17,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Multifocal fibrosclerosis","text":"Phenotype: Multifocal fibrosclerosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.17<br>N cases: 161<br>N controls: 365533"}
{"pvalue":0.32,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Muscle wasting and atrophy, not elsewhere classified","text":"Phenotype: Muscle wasting and atrophy, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.32<br>N cases: 163<br>N controls: 275212"}
{"pvalue":0.768,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other specified disorders of muscle","text":"Phenotype: Other specified disorders of muscle<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.768<br>N cases: 805<br>N controls: 275212"}
{"pvalue":0.617,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Disorders of muscles","text":"Phenotype: Disorders of muscles<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.617<br>N cases: 3008<br>N controls: 275212"}
{"pvalue":0.777,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Muscle strain","text":"Phenotype: Muscle strain<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.777<br>N cases: 815<br>N controls: 275212"}
{"pvalue":0.609,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Contracture of muscle","text":"Phenotype: Contracture of muscle<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.609<br>N cases: 97<br>N controls: 275212"}
{"pvalue":0.0815,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other disorders of the musculoskeletal system and connective tissue","text":"Phenotype: Other disorders of the musculoskeletal system and connective tissue<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0815<br>N cases: 3974<br>N controls: 373303"}
{"pvalue":0.616,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Myalgia","text":"Phenotype: Myalgia<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.616<br>N cases: 7024<br>N controls: 275212"}
{"pvalue":0.51,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Myositis","text":"Phenotype: Myositis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.51<br>N cases: 692<br>N controls: 275212"}
{"pvalue":0.109,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Necrotizing fasciitis","text":"Phenotype: Necrotizing fasciitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.109<br>N cases: 101<br>N controls: 275212"}
{"pvalue":0.852,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other specified/unspecified necrotizing vasculopathies","text":"Phenotype: Other specified/unspecified necrotizing vasculopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.852<br>N cases: 368<br>N controls: 365533"}
{"pvalue":0.433,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Neuralgia and neuritis, unspecified","text":"Phenotype: Neuralgia and neuritis, unspecified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.433<br>N cases: 1413<br>N controls: 275212"}
{"pvalue":0.15,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Olecranon bursitis","text":"Phenotype: Olecranon bursitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.15<br>N cases: 1681<br>N controls: 275212"}
{"pvalue":0.973,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Osteopathies and chondropathies","text":"Phenotype: Osteopathies and chondropathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.973<br>N cases: 19263<br>N controls: 358014"}
{"pvalue":0.848,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other osteochondropathies","text":"Phenotype: Other osteochondropathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.848<br>N cases: 2091<br>N controls: 370709"}
{"pvalue":0.244,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Osteomalacia","text":"Phenotype: Osteomalacia<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.244<br>N cases: 224<br>N controls: 358014"}
{"pvalue":0.828,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Osteomyelitis","text":"Phenotype: Osteomyelitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.828<br>N cases: 1758<br>N controls: 358014"}
{"pvalue":0.776,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Osteomyelitis of vertebra","text":"Phenotype: Osteomyelitis of vertebra<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.776<br>N cases: 89<br>N controls: 270964"}
{"pvalue":0.719,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Osteonecrosis","text":"Phenotype: Osteonecrosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.719<br>N cases: 1385<br>N controls: 358014"}
{"pvalue":0.929,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Osteopathy in diseases classified elsewhere","text":"Phenotype: Osteopathy in diseases classified elsewhere<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.929<br>N cases: 166<br>N controls: 358014"}
{"pvalue":0.243,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Osteoporosis","text":"Phenotype: Osteoporosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.243<br>N cases: 7300<br>N controls: 358014"}
{"pvalue":0.95,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other disorders of bone","text":"Phenotype: Other disorders of bone<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.95<br>N cases: 6568<br>N controls: 358014"}
{"pvalue":0.333,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other joint disorders","text":"Phenotype: Other joint disorders<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.333<br>N cases: 81676<br>N controls: 240862"}
{"pvalue":0.689,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other overlap syndromes","text":"Phenotype: Other overlap syndromes<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.689<br>N cases: 501<br>N controls: 365533"}
{"pvalue":0.571,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other/unspecified soft tissue disorders related to use, overuse and pressure","text":"Phenotype: Other/unspecified soft tissue disorders related to use, overuse and pressure<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.571<br>N cases: 800<br>N controls: 275212"}
{"pvalue":0.408,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Paget disease","text":"Phenotype: Paget disease<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.408<br>N cases: 115<br>N controls: 358014"}
{"pvalue":0.998,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Palindromic rheumatism","text":"Phenotype: Palindromic rheumatism<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.998<br>N cases: 285<br>N controls: 240862"}
{"pvalue":0.99,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Panniculitis affecting regions of neck and back","text":"Phenotype: Panniculitis affecting regions of neck and back<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.99<br>N cases: 1115<br>N controls: 270964"}
{"pvalue":0.671,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Panniculitis, unspecified","text":"Phenotype: Panniculitis, unspecified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.671<br>N cases: 279<br>N controls: 275212"}
{"pvalue":0.237,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Recurrent dislocation of patella","text":"Phenotype: Recurrent dislocation of patella<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.237<br>N cases: 1645<br>N controls: 240862"}
{"pvalue":0.997,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other disorders of patella","text":"Phenotype: Other disorders of patella<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.997<br>N cases: 6333<br>N controls: 240862"}
{"pvalue":0.34,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Patellar tendinitis","text":"Phenotype: Patellar tendinitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.34<br>N cases: 439<br>N controls: 270964"}
{"pvalue":0.186,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Peroneal tendinitis","text":"Phenotype: Peroneal tendinitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.186<br>N cases: 361<br>N controls: 270964"}
{"pvalue":0.944,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Plantar fascial fibromatosis","text":"Phenotype: Plantar fascial fibromatosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.944<br>N cases: 2768<br>N controls: 275212"}
{"pvalue":0.219,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Polyarteritis nodosa","text":"Phenotype: Polyarteritis nodosa<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.219<br>N cases: 185<br>N controls: 365533"}
{"pvalue":0.647,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Polyarteritis nodosa and related conditions","text":"Phenotype: Polyarteritis nodosa and related conditions<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.647<br>N cases: 373<br>N controls: 365533"}
{"pvalue":0.0951,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Polyarthritis, unspecified","text":"Phenotype: Polyarthritis, unspecified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0951<br>N cases: 1047<br>N controls: 240862"}
{"pvalue":0.0458,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Polyarthropathies","text":"Phenotype: Polyarthropathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0458<br>N cases: 32199<br>N controls: 240862"}
{"pvalue":0.123,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Polymyalgia rheumatica","text":"Phenotype: Polymyalgia rheumatica<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.123<br>N cases: 3501<br>N controls: 365533"}
{"pvalue":0.0336,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Polymyositis","text":"Phenotype: Polymyositis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0336<br>N cases: 225<br>N controls: 365533"}
{"pvalue":0.541,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Postprocedural musculoskeletal disorders, not elsewhere classified","text":"Phenotype: Postprocedural musculoskeletal disorders, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.541<br>N cases: 1725<br>N controls: 373303"}
{"pvalue":0.991,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Prepatellar bursitis","text":"Phenotype: Prepatellar bursitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.991<br>N cases: 1210<br>N controls: 275212"}
{"pvalue":0.492,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Psoas tendinitis","text":"Phenotype: Psoas tendinitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.492<br>N cases: 105<br>N controls: 270964"}
{"pvalue":0.011,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Psoriatic arthropathies","text":"Phenotype: Psoriatic arthropathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.011<br>N cases: 3186<br>N controls: 240862"}
{"pvalue":0.0287,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Pyogenic arthritis","text":"Phenotype: Pyogenic arthritis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0287<br>N cases: 2029<br>N controls: 240862"}
{"pvalue":0.144,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Radiculopathy","text":"Phenotype: Radiculopathy<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.144<br>N cases: 5550<br>N controls: 270964"}
{"pvalue":0.734,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Reactive arthropathies","text":"Phenotype: Reactive arthropathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.734<br>N cases: 2813<br>N controls: 240862"}
{"pvalue":0.808,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Recurrent dislocation and subluxation of joint","text":"Phenotype: Recurrent dislocation and subluxation of joint<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.808<br>N cases: 2240<br>N controls: 240862"}
{"pvalue":0.00169,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Rheumatoid arthritis","text":"Phenotype: Rheumatoid arthritis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00169<br>N cases: 12555<br>N controls: 240862"}
{"pvalue":0.32,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Rheumatism, unspecified","text":"Phenotype: Rheumatism, unspecified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.32<br>N cases: 4674<br>N controls: 275212"}
{"pvalue":0.243,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Rotator cuff syndrome","text":"Phenotype: Rotator cuff syndrome<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.243<br>N cases: 24061<br>N controls: 275212"}
{"pvalue":0.695,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other rupture of muscle","text":"Phenotype: Other rupture of muscle<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.695<br>N cases: 148<br>N controls: 275212"}
{"pvalue":0.84,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Sacrococcygeal disorders, not elsewhere classified","text":"Phenotype: Sacrococcygeal disorders, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.84<br>N cases: 872<br>N controls: 270964"}
{"pvalue":0.12,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Sacroiliitis, not elsewhere classified","text":"Phenotype: Sacroiliitis, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.12<br>N cases: 1394<br>N controls: 270964"}
{"pvalue":0.0981,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Sciatica+with lumbago","text":"Phenotype: Sciatica+with lumbago<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0981<br>N cases: 18569<br>N controls: 270964"}
{"pvalue":0.048,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Scoliosis","text":"Phenotype: Scoliosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.048<br>N cases: 2529<br>N controls: 270964"}
{"pvalue":0.0766,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Short Achilles tendon (acquired)","text":"Phenotype: Short Achilles tendon (acquired)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0766<br>N cases: 652<br>N controls: 275212"}
{"pvalue":0.0285,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Bursitis of shoulder","text":"Phenotype: Bursitis of shoulder<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0285<br>N cases: 651<br>N controls: 275212"}
{"pvalue":0.489,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Shoulder lesions","text":"Phenotype: Shoulder lesions<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.489<br>N cases: 34594<br>N controls: 275212"}
{"pvalue":0.159,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other shoulder lesions","text":"Phenotype: Other shoulder lesions<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.159<br>N cases: 2663<br>N controls: 275212"}
{"pvalue":0.986,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Sicca syndrome [Sjögren]","text":"Phenotype: Sicca syndrome [Sjögren]<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.986<br>N cases: 2495<br>N controls: 365533"}
{"pvalue":0.0364,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Soft tissue disorders related to use, overuse and pressure","text":"Phenotype: Soft tissue disorders related to use, overuse and pressure<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0364<br>N cases: 8236<br>N controls: 275212"}
{"pvalue":0.922,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Soft tissue disorders","text":"Phenotype: Soft tissue disorders<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.922<br>N cases: 102065<br>N controls: 275212"}
{"pvalue":0.956,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other specified/unspecified soft tissue disorders","text":"Phenotype: Other specified/unspecified soft tissue disorders<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.956<br>N cases: 1475<br>N controls: 275212"}
{"pvalue":0.681,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other soft tissue disorders, not elsewhere classified","text":"Phenotype: Other soft tissue disorders, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.681<br>N cases: 43190<br>N controls: 275212"}
{"pvalue":0.615,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Spinal osteochondrosis","text":"Phenotype: Spinal osteochondrosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.615<br>N cases: 318<br>N controls: 270964"}
{"pvalue":0.884,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Spinal enthesopathy","text":"Phenotype: Spinal enthesopathy<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.884<br>N cases: 1145<br>N controls: 270964"}
{"pvalue":0.698,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Spinal instabilities","text":"Phenotype: Spinal instabilities<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.698<br>N cases: 839<br>N controls: 270964"}
{"pvalue":0.00019,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Spinal stenosis","text":"Phenotype: Spinal stenosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.000189<br>N cases: 18989<br>N controls: 270964"}
{"pvalue":0.75,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other specified/unspecified inflammatory spondylopathies","text":"Phenotype: Other specified/unspecified inflammatory spondylopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.75<br>N cases: 1448<br>N controls: 270964"}
{"pvalue":0.11,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Spondylolisthesis/Spondylolysis","text":"Phenotype: Spondylolisthesis/Spondylolysis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.11<br>N cases: 5766<br>N controls: 270964"}
{"pvalue":0.515,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Spondylopathies in diseases classified elsewhere","text":"Phenotype: Spondylopathies in diseases classified elsewhere<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.515<br>N cases: 286<br>N controls: 270964"}
{"pvalue":0.0362,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Spondylopathies","text":"Phenotype: Spondylopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0362<br>N cases: 38276<br>N controls: 270964"}
{"pvalue":0.914,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Other specified/unspecified spondylopathies","text":"Phenotype: Other specified/unspecified spondylopathies<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.914<br>N cases: 693<br>N controls: 270964"}
{"pvalue":0.00577,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Spondylosis","text":"Phenotype: Spondylosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00577<br>N cases: 19892<br>N controls: 270964"}
{"pvalue":0.515,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Spontaneous rupture of synovium and tendon","text":"Phenotype: Spontaneous rupture of synovium and tendon<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.515<br>N cases: 2313<br>N controls: 275212"}
{"pvalue":0.388,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Synovial hypertrophy, not elsewhere classified","text":"Phenotype: Synovial hypertrophy, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.388<br>N cases: 273<br>N controls: 275212"}
{"pvalue":0.442,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Disorders of synovium and tendon","text":"Phenotype: Disorders of synovium and tendon<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.442<br>N cases: 20492<br>N controls: 275212"}
{"pvalue":0.0588,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Disorders of synovium and tendon in diseases classified elsewhere","text":"Phenotype: Disorders of synovium and tendon in diseases classified elsewhere<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0588<br>N cases: 529<br>N controls: 275212"}
{"pvalue":0.386,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Systemic disorders of connective tissue in diseases classified elsewhere","text":"Phenotype: Systemic disorders of connective tissue in diseases classified elsewhere<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.386<br>N cases: 113<br>N controls: 365533"}
{"pvalue":0.421,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Systemic connective tissue disorders","text":"Phenotype: Systemic connective tissue disorders<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.421<br>N cases: 11744<br>N controls: 365533"}
{"pvalue":0.486,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Systemic sclerosis","text":"Phenotype: Systemic sclerosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.486<br>N cases: 619<br>N controls: 365533"}
{"pvalue":0.366,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Temporal arteritis","text":"Phenotype: Temporal arteritis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.366<br>N cases: 891<br>N controls: 365533"}
{"pvalue":0.686,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Oher contracture of tendon (sheath)","text":"Phenotype: Oher contracture of tendon (sheath)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.686<br>N cases: 91<br>N controls: 275212"}
{"pvalue":0.245,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other/unspecified synovitis and tenosynovitis","text":"Phenotype: Other/unspecified synovitis and tenosynovitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.245<br>N cases: 3704<br>N controls: 275212"}
{"pvalue":0.62,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Pain in thoracic spine","text":"Phenotype: Pain in thoracic spine<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.62<br>N cases: 4651<br>N controls: 270964"}
{"pvalue":0.23,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Tibial collateral bursitis [Pellegrini-Stieda]","text":"Phenotype: Tibial collateral bursitis [Pellegrini-Stieda]<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.23<br>N cases: 270<br>N controls: 270964"}
{"pvalue":0.658,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Chondrocostal junction syndrome [Tietze]","text":"Phenotype: Chondrocostal junction syndrome [Tietze]<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.658<br>N cases: 912<br>N controls: 370709"}
{"pvalue":0.256,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Other deformities of toe(s)","text":"Phenotype: Other deformities of toe(s)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.256<br>N cases: 975<br>N controls: 240862"}
{"pvalue":0.18,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Torticollis","text":"Phenotype: Torticollis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.18<br>N cases: 460<br>N controls: 270964"}
{"pvalue":0.151,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Transient synovitis","text":"Phenotype: Transient synovitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.151<br>N cases: 209<br>N controls: 275212"}
{"pvalue":0.735,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Trigger finger","text":"Phenotype: Trigger finger<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.735<br>N cases: 4284<br>N controls: 275212"}
{"pvalue":0.104,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Trochanteric bursitis","text":"Phenotype: Trochanteric bursitis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.104<br>N cases: 3529<br>N controls: 275212"}
{"pvalue":0.264,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Valgus deformity, not elsewhere classified","text":"Phenotype: Valgus deformity, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.264<br>N cases: 191<br>N controls: 240862"}
{"pvalue":0.584,"sign":-1,"group":"M13: Musculoskeletal system diseases","label":"Varus deformity, not elsewhere classified","text":"Phenotype: Varus deformity, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.584<br>N cases: 298<br>N controls: 240862"}
{"pvalue":0.0122,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Collapsed vertebra, not elsewhere classified","text":"Phenotype: Collapsed vertebra, not elsewhere classified<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0122<br>N cases: 193<br>N controls: 270964"}
{"pvalue":0.831,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Villonodular synovitis (pigmented)","text":"Phenotype: Villonodular synovitis (pigmented)<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.831<br>N cases: 212<br>N controls: 240862"}
{"pvalue":0.809,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Wegener granulomatosis","text":"Phenotype: Wegener granulomatosis<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.809<br>N cases: 413<br>N controls: 365533"}
{"pvalue":0.783,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Degenerative macular diseases, drug-induced","text":"Phenotype: Degenerative macular diseases, drug-induced<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.783<br>N cases: 84<br>N controls: 377193"}
{"pvalue":0.173,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Degenerative macular diseases","text":"Phenotype: Degenerative macular diseases<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.173<br>N cases: 3473<br>N controls: 344569"}
{"pvalue":0.382,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Macular cyst","text":"Phenotype: Macular cyst<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.382<br>N cases: 491<br>N controls: 344569"}
{"pvalue":0.139,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Macular hole","text":"Phenotype: Macular hole<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.139<br>N cases: 1266<br>N controls: 344569"}
{"pvalue":0.695,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Macular pucker","text":"Phenotype: Macular pucker<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.695<br>N cases: 3576<br>N controls: 344569"}
{"pvalue":0.236,"sign":1,"group":"G6: Nervous system diseases","label":"Migraine, unspecified, drug-induced","text":"Phenotype: Migraine, unspecified, drug-induced<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.236<br>N cases: 186<br>N controls: 377091"}
{"pvalue":0.761,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other abnormal uterine and caginal bleeding","text":"Phenotype: Other abnormal uterine and caginal bleeding<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.761<br>N cases: 10319<br>N controls: 107564"}
{"pvalue":0.528,"sign":1,"group":"N14: Genitourinary system diseases","label":"Acute nephritic syndrome","text":"Phenotype: Acute nephritic syndrome<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.528<br>N cases: 581<br>N controls: 371635"}
{"pvalue":0.0735,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Acute renal failure","text":"Phenotype: Acute renal failure<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0735<br>N cases: 5908<br>N controls: 363177"}
{"pvalue":0.669,"sign":1,"group":"N14: Genitourinary system diseases","label":"Amenorrhoea","text":"Phenotype: Amenorrhoea<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.669<br>N cases: 2220<br>N controls: 107564"}
{"pvalue":0.177,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Abscess of Bartholin gland","text":"Phenotype: Abscess of Bartholin gland<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.177<br>N cases: 699<br>N controls: 188295"}
{"pvalue":0.506,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Cyst of Bartholin Gland","text":"Phenotype: Cyst of Bartholin Gland<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.506<br>N cases: 1055<br>N controls: 188295"}
{"pvalue":0.643,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other and unspecified disease of Bartholin gland","text":"Phenotype: Other and unspecified disease of Bartholin gland<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.643<br>N cases: 807<br>N controls: 188295"}
{"pvalue":0.52,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Benign mammary dysplasia","text":"Phenotype: Benign mammary dysplasia<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.52<br>N cases: 4329<br>N controls: 193973"}
{"pvalue":0.797,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Other disorders of breast","text":"Phenotype: Other disorders of breast<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.797<br>N cases: 3450<br>N controls: 193973"}
{"pvalue":0.145,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Disorders of breast","text":"Phenotype: Disorders of breast<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.145<br>N cases: 16897<br>N controls: 193973"}
{"pvalue":0.201,"sign":1,"group":"N14: Genitourinary system diseases","label":"Calculus of kidney and ureter","text":"Phenotype: Calculus of kidney and ureter<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.201<br>N cases: 9713<br>N controls: 366693"}
{"pvalue":0.401,"sign":1,"group":"N14: Genitourinary system diseases","label":"Calculus of lower urinary tract","text":"Phenotype: Calculus of lower urinary tract<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.401<br>N cases: 1398<br>N controls: 366693"}
{"pvalue":0.355,"sign":1,"group":"N14: Genitourinary system diseases","label":"All dysplastic lesions of the cervix uteri","text":"Phenotype: All dysplastic lesions of the cervix uteri<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.355<br>N cases: 8025<br>N controls: 202845"}
{"pvalue":0.32,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Dysplastic lesion of unknown severity of the cervix uteri","text":"Phenotype: Dysplastic lesion of unknown severity of the cervix uteri<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.32<br>N cases: 242<br>N controls: 210628"}
{"pvalue":0.879,"sign":1,"group":"N14: Genitourinary system diseases","label":"HSIL lesion of the cervix uteri","text":"Phenotype: HSIL lesion of the cervix uteri<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.879<br>N cases: 5459<br>N controls: 205411"}
{"pvalue":0.116,"sign":1,"group":"N14: Genitourinary system diseases","label":"LSIL lesion of the cervix uteri","text":"Phenotype: LSIL lesion of the cervix uteri<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.116<br>N cases: 3207<br>N controls: 207663"}
{"pvalue":0.155,"sign":1,"group":"N14: Genitourinary system diseases","label":"Chronic nephritic syndrome","text":"Phenotype: Chronic nephritic syndrome<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.155<br>N cases: 1098<br>N controls: 371635"}
{"pvalue":0.583,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Chronic kidney disease","text":"Phenotype: Chronic kidney disease<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.583<br>N cases: 9073<br>N controls: 363177"}
{"pvalue":0.661,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Chronic tubulo-interstitial nephritis","text":"Phenotype: Chronic tubulo-interstitial nephritis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.661<br>N cases: 1127<br>N controls: 338942"}
{"pvalue":0.125,"sign":1,"group":"N14: Genitourinary system diseases","label":"Cystitis","text":"Phenotype: Cystitis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.125<br>N cases: 18080<br>N controls: 328001"}
{"pvalue":0.816,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Cyst of kidney","text":"Phenotype: Cyst of kidney<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.816<br>N cases: 1696<br>N controls: 373761"}
{"pvalue":0.211,"sign":1,"group":"N14: Genitourinary system diseases","label":"Dialysis","text":"Phenotype: Dialysis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.211<br>N cases: 1004<br>N controls: 363177"}
{"pvalue":0.305,"sign":1,"group":"N14: Genitourinary system diseases","label":"Disorders resulting from impaired renal tubular function","text":"Phenotype: Disorders resulting from impaired renal tubular function<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.305<br>N cases: 859<br>N controls: 373761"}
{"pvalue":0.472,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Endometriosis diagnosis and infertility diagnosis occurring together","text":"Phenotype: Endometriosis diagnosis and infertility diagnosis occurring together<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.472<br>N cases: 3206<br>N controls: 201035"}
{"pvalue":0.606,"sign":1,"group":"N14: Genitourinary system diseases","label":"Endometriosis ASRM stages 1,2","text":"Phenotype: Endometriosis ASRM stages 1,2<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.606<br>N cases: 5769<br>N controls: 205101"}
{"pvalue":0.877,"sign":1,"group":"N14: Genitourinary system diseases","label":"Endometriosis ASRM stages 3,4","text":"Phenotype: Endometriosis ASRM stages 3,4<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.877<br>N cases: 7574<br>N controls: 203296"}
{"pvalue":0.306,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Deep endometriosis","text":"Phenotype: Deep endometriosis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.306<br>N cases: 2856<br>N controls: 203296"}
{"pvalue":0.498,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Endometriosis of fallopian tube","text":"Phenotype: Endometriosis of fallopian tube<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.498<br>N cases: 213<br>N controls: 107564"}
{"pvalue":0.28,"sign":1,"group":"N14: Genitourinary system diseases","label":"Endometriosis","text":"Phenotype: Endometriosis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.28<br>N cases: 15088<br>N controls: 107564"}
{"pvalue":0.232,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Endometriosis of intestine","text":"Phenotype: Endometriosis of intestine<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.232<br>N cases: 436<br>N controls: 107564"}
{"pvalue":0.573,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Unspecified/other endometriosis","text":"Phenotype: Unspecified/other endometriosis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.573<br>N cases: 2982<br>N controls: 107564"}
{"pvalue":0.694,"sign":1,"group":"N14: Genitourinary system diseases","label":"Endometriosis of ovary","text":"Phenotype: Endometriosis of ovary<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.694<br>N cases: 5867<br>N controls: 107564"}
{"pvalue":0.44,"sign":1,"group":"N14: Genitourinary system diseases","label":"Endometriosis of pelvic peritoneum","text":"Phenotype: Endometriosis of pelvic peritoneum<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.44<br>N cases: 5628<br>N controls: 107564"}
{"pvalue":0.652,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Endometriosis of rectovaginal septum and vagina","text":"Phenotype: Endometriosis of rectovaginal septum and vagina<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.652<br>N cases: 2456<br>N controls: 107564"}
{"pvalue":0.168,"sign":1,"group":"N14: Genitourinary system diseases","label":"Adenomyosis (Endometriosis of uterus)","text":"Phenotype: Adenomyosis (Endometriosis of uterus)<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.168<br>N cases: 4267<br>N controls: 107564"}
{"pvalue":0.953,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Erosion and ectropion of cervix uteri","text":"Phenotype: Erosion and ectropion of cervix uteri<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.953<br>N cases: 830<br>N controls: 107564"}
{"pvalue":0.0597,"sign":1,"group":"N14: Genitourinary system diseases","label":"Inflammatory diseases of female pelvic organs","text":"Phenotype: Inflammatory diseases of female pelvic organs<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0597<br>N cases: 22575<br>N controls: 188295"}
{"pvalue":0.237,"sign":1,"group":"N14: Genitourinary system diseases","label":"All dysplastic lesions of the cervix uteri, vagina or vulva","text":"Phenotype: All dysplastic lesions of the cervix uteri, vagina or vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.237<br>N cases: 9227<br>N controls: 201643"}
{"pvalue":0.43,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Dysplastic lesion of unknown severity in the cervix uteri, vagina or vulva","text":"Phenotype: Dysplastic lesion of unknown severity in the cervix uteri, vagina or vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.43<br>N cases: 302<br>N controls: 210568"}
{"pvalue":0.626,"sign":1,"group":"N14: Genitourinary system diseases","label":"HSIL lesion of the cervix uteri, vagina or vulva","text":"Phenotype: HSIL lesion of the cervix uteri, vagina or vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.626<br>N cases: 5996<br>N controls: 204874"}
{"pvalue":0.0843,"sign":1,"group":"N14: Genitourinary system diseases","label":"LSIL lesion of the cervix uteri, vagina or vulva","text":"Phenotype: LSIL lesion of the cervix uteri, vagina or vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0843<br>N cases: 4102<br>N controls: 206768"}
{"pvalue":0.114,"sign":1,"group":"N14: Genitourinary system diseases","label":"Noninflammatory disorders of female genital tract","text":"Phenotype: Noninflammatory disorders of female genital tract<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.114<br>N cases: 103306<br>N controls: 107564"}
{"pvalue":0.283,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Female infertility","text":"Phenotype: Female infertility<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.283<br>N cases: 13142<br>N controls: 107564"}
{"pvalue":0.943,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Fistulae involving female genital tract","text":"Phenotype: Fistulae involving female genital tract<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.943<br>N cases: 424<br>N controls: 107564"}
{"pvalue":0.375,"sign":1,"group":"N14: Genitourinary system diseases","label":"Pain and other conditions associated with female genital organs and menstrual cycle","text":"Phenotype: Pain and other conditions associated with female genital organs and menstrual cycle<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.375<br>N cases: 6976<br>N controls: 107564"}
{"pvalue":0.258,"sign":1,"group":"N14: Genitourinary system diseases","label":"Female genital prolapse","text":"Phenotype: Female genital prolapse<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.258<br>N cases: 17150<br>N controls: 107564"}
{"pvalue":0.121,"sign":1,"group":"N14: Genitourinary system diseases","label":"Female pelvic inflammatory disorders in diseases classified elsewhere","text":"Phenotype: Female pelvic inflammatory disorders in diseases classified elsewhere<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.121<br>N cases: 98<br>N controls: 188295"}
{"pvalue":0.173,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Female infertility, associated with anovulation","text":"Phenotype: Female infertility, associated with anovulation<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.173<br>N cases: 2441<br>N controls: 107564"}
{"pvalue":0.32,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Female infertility, cervigal, vaginal, other or unspecified origin","text":"Phenotype: Female infertility, cervigal, vaginal, other or unspecified origin<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.32<br>N cases: 11348<br>N controls: 107564"}
{"pvalue":0.961,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Female infertility, tubal origin","text":"Phenotype: Female infertility, tubal origin<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.961<br>N cases: 1483<br>N controls: 107564"}
{"pvalue":0.67,"sign":1,"group":"N14: Genitourinary system diseases","label":"Female infertility, uterine origin","text":"Phenotype: Female infertility, uterine origin<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.67<br>N cases: 99<br>N controls: 107564"}
{"pvalue":0.167,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Galactorrhea","text":"Phenotype: Galactorrhea<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.167<br>N cases: 272<br>N controls: 193973"}
{"pvalue":0.793,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other disorders of the genitourinary system","text":"Phenotype: Other disorders of the genitourinary system<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.793<br>N cases: 3607<br>N controls: 373670"}
{"pvalue":0.454,"sign":1,"group":"N14: Genitourinary system diseases","label":"Glomerular disorders in diseases classified elsewhere","text":"Phenotype: Glomerular disorders in diseases classified elsewhere<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.454<br>N cases: 3374<br>N controls: 371635"}
{"pvalue":0.107,"sign":1,"group":"N14: Genitourinary system diseases","label":"Glomerulonephritis","text":"Phenotype: Glomerulonephritis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.107<br>N cases: 1605<br>N controls: 375672"}
{"pvalue":0.825,"sign":1,"group":"N14: Genitourinary system diseases","label":"Glomerular diseases","text":"Phenotype: Glomerular diseases<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.825<br>N cases: 5642<br>N controls: 371635"}
{"pvalue":0.339,"sign":1,"group":"N14: Genitourinary system diseases","label":"Habitual aborter","text":"Phenotype: Habitual aborter<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.339<br>N cases: 571<br>N controls: 107564"}
{"pvalue":0.366,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Henoch-Schönlein purpura nephritis (HSPN)","text":"Phenotype: Henoch-Schönlein purpura nephritis (HSPN)<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.366<br>N cases: 94<br>N controls: 377183"}
{"pvalue":0.0448,"sign":1,"group":"N14: Genitourinary system diseases","label":"Hydrocele","text":"Phenotype: Hydrocele<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0448<br>N cases: 5221<br>N controls: 119297"}
{"pvalue":0.0388,"sign":1,"group":"N14: Genitourinary system diseases","label":"Hydronephrosis","text":"Phenotype: Hydronephrosis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0388<br>N cases: 3252<br>N controls: 338942"}
{"pvalue":0.752,"sign":1,"group":"N14: Genitourinary system diseases","label":"Hypertrophy of breast in women and men","text":"Phenotype: Hypertrophy of breast in women and men<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.752<br>N cases: 6105<br>N controls: 359487"}
{"pvalue":0.69,"sign":1,"group":"N14: Genitourinary system diseases","label":"Hypertrophy of breast","text":"Phenotype: Hypertrophy of breast<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.69<br>N cases: 5212<br>N controls: 193973"}
{"pvalue":0.0229,"sign":1,"group":"N14: Genitourinary system diseases","label":"IgA nephropathy (IgA glomerulonephritis)","text":"Phenotype: IgA nephropathy (IgA glomerulonephritis)<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0229<br>N cases: 592<br>N controls: 376685"}
{"pvalue":0.867,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Impotence","text":"Phenotype: Impotence<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.867<br>N cases: 1264<br>N controls: 119297"}
{"pvalue":0.819,"sign":1,"group":"N14: Genitourinary system diseases","label":"Inflammatory disease of cervix uteri","text":"Phenotype: Inflammatory disease of cervix uteri<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.819<br>N cases: 1847<br>N controls: 188295"}
{"pvalue":0.92,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Inflammatory disorders of male genital organs, not elsewhere classified","text":"Phenotype: Inflammatory disorders of male genital organs, not elsewhere classified<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.92<br>N cases: 357<br>N controls: 119297"}
{"pvalue":1,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Inflammatory disorders of breast","text":"Phenotype: Inflammatory disorders of breast<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 1<br>N cases: 1668<br>N controls: 193973"}
{"pvalue":0.696,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Inflammatory disease of uterus","text":"Phenotype: Inflammatory disease of uterus<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.696<br>N cases: 4337<br>N controls: 188295"}
{"pvalue":0.219,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Isolated proteinuria with specified morphological lesion","text":"Phenotype: Isolated proteinuria with specified morphological lesion<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.219<br>N cases: 288<br>N controls: 371635"}
{"pvalue":0.947,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other disorders of kidney and ureter","text":"Phenotype: Other disorders of kidney and ureter<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.947<br>N cases: 3516<br>N controls: 373761"}
{"pvalue":0.0265,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Unspecified lump in breast","text":"Phenotype: Unspecified lump in breast<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0265<br>N cases: 4681<br>N controls: 193973"}
{"pvalue":0.784,"sign":1,"group":"N14: Genitourinary system diseases","label":"Diseases of male genital organs","text":"Phenotype: Diseases of male genital organs<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.784<br>N cases: 47110<br>N controls: 119297"}
{"pvalue":0.685,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Disorders of male genital organs in diseases classified elsewhere","text":"Phenotype: Disorders of male genital organs in diseases classified elsewhere<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.685<br>N cases: 142<br>N controls: 119297"}
{"pvalue":0.0075,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Male infertility","text":"Phenotype: Male infertility<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0075<br>N cases: 1271<br>N controls: 119297"}
{"pvalue":0.0328,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other menopausal disorders","text":"Phenotype: Other menopausal disorders<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0328<br>N cases: 4777<br>N controls: 107564"}
{"pvalue":0.408,"sign":1,"group":"N14: Genitourinary system diseases","label":"Menorrhagia","text":"Phenotype: Menorrhagia<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.408<br>N cases: 21496<br>N controls: 107564"}
{"pvalue":0.0198,"sign":1,"group":"N14: Genitourinary system diseases","label":"Irregular menses","text":"Phenotype: Irregular menses<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0198<br>N cases: 17228<br>N controls: 179322"}
{"pvalue":0.0815,"sign":1,"group":"N14: Genitourinary system diseases","label":"Excessive, frequent and irregular menstruation","text":"Phenotype: Excessive, frequent and irregular menstruation<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0815<br>N cases: 36824<br>N controls: 107564"}
{"pvalue":0.241,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Unspecified nephritic syndrome","text":"Phenotype: Unspecified nephritic syndrome<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.241<br>N cases: 584<br>N controls: 371635"}
{"pvalue":0.495,"sign":1,"group":"N14: Genitourinary system diseases","label":"Nephrotic syndrome","text":"Phenotype: Nephrotic syndrome<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.495<br>N cases: 853<br>N controls: 371635"}
{"pvalue":0.24,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Neuromuscular dysfunction of bladder","text":"Phenotype: Neuromuscular dysfunction of bladder<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.24<br>N cases: 2618<br>N controls: 328001"}
{"pvalue":0.0772,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other obstructive and reflux uropathy","text":"Phenotype: Other obstructive and reflux uropathy<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0772<br>N cases: 3832<br>N controls: 338942"}
{"pvalue":0.176,"sign":1,"group":"N14: Genitourinary system diseases","label":"Oligomenorrhoea","text":"Phenotype: Oligomenorrhoea<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.176<br>N cases: 1065<br>N controls: 107564"}
{"pvalue":0.0463,"sign":1,"group":"N14: Genitourinary system diseases","label":"Orchitis and epididymitis","text":"Phenotype: Orchitis and epididymitis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0463<br>N cases: 2688<br>N controls: 119297"}
{"pvalue":0.464,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other disorders of  bladder","text":"Phenotype: Other disorders of  bladder<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.464<br>N cases: 3435<br>N controls: 328001"}
{"pvalue":0.682,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Other disorders of male genital organs","text":"Phenotype: Other disorders of male genital organs<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.682<br>N cases: 936<br>N controls: 119297"}
{"pvalue":0.62,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Other specified disorders of kidney and ureter","text":"Phenotype: Other specified disorders of kidney and ureter<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.62<br>N cases: 875<br>N controls: 373761"}
{"pvalue":0.00967,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other female pelvic inflammatory diseases","text":"Phenotype: Other female pelvic inflammatory diseases<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00967<br>N cases: 5117<br>N controls: 188295"}
{"pvalue":0.775,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other inflammation of vagina/vulva","text":"Phenotype: Other inflammation of vagina/vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.775<br>N cases: 1013<br>N controls: 188295"}
{"pvalue":0.975,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other noninflammatory disorders of cervix uteri","text":"Phenotype: Other noninflammatory disorders of cervix uteri<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.975<br>N cases: 1426<br>N controls: 107564"}
{"pvalue":0.654,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other and unspecified noninflammatory disorders of ovary, fallopian tube and broad ligament","text":"Phenotype: Other and unspecified noninflammatory disorders of ovary, fallopian tube and broad ligament<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.654<br>N cases: 778<br>N controls: 107564"}
{"pvalue":0.583,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other noninflammatory disorders of uterus, except cervix","text":"Phenotype: Other noninflammatory disorders of uterus, except cervix<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.583<br>N cases: 8752<br>N controls: 107564"}
{"pvalue":0.949,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Other noninflammatory disorders of vagina","text":"Phenotype: Other noninflammatory disorders of vagina<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.949<br>N cases: 2358<br>N controls: 107564"}
{"pvalue":0.0573,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other noninflammatory disorders of vulva and perineum","text":"Phenotype: Other noninflammatory disorders of vulva and perineum<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0573<br>N cases: 2660<br>N controls: 107564"}
{"pvalue":0.883,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other disorders of penis","text":"Phenotype: Other disorders of penis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.883<br>N cases: 2643<br>N controls: 119297"}
{"pvalue":0.684,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Ovarian hyperstimulation (induction)","text":"Phenotype: Ovarian hyperstimulation (induction)<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.684<br>N cases: 436<br>N controls: 197728"}
{"pvalue":0.0958,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Torsion of ovary, ovarian pedicle and fallopian tube","text":"Phenotype: Torsion of ovary, ovarian pedicle and fallopian tube<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0958<br>N cases: 642<br>N controls: 107564"}
{"pvalue":0.0123,"sign":1,"group":"N14: Genitourinary system diseases","label":"Ovarian cyst","text":"Phenotype: Ovarian cyst<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0123<br>N cases: 20750<br>N controls: 107564"}
{"pvalue":0.512,"sign":1,"group":"N14: Genitourinary system diseases","label":"Redundant prepuce, phimosis and paraphimosis","text":"Phenotype: Redundant prepuce, phimosis and paraphimosis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.512<br>N cases: 6859<br>N controls: 119297"}
{"pvalue":0.778,"sign":1,"group":"N14: Genitourinary system diseases","label":"Polyp of the female genital tract","text":"Phenotype: Polyp of the female genital tract<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.778<br>N cases: 14324<br>N controls: 107564"}
{"pvalue":0.653,"sign":1,"group":"N14: Genitourinary system diseases","label":"Postmenopausal atrophic vaginitis","text":"Phenotype: Postmenopausal atrophic vaginitis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.653<br>N cases: 2534<br>N controls: 107564"}
{"pvalue":0.73,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Postmenopausal bleeding","text":"Phenotype: Postmenopausal bleeding<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.73<br>N cases: 11582<br>N controls: 107564"}
{"pvalue":0.878,"sign":1,"group":"N14: Genitourinary system diseases","label":"Premenstrual syndrome","text":"Phenotype: Premenstrual syndrome<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.878<br>N cases: 247<br>N controls: 107564"}
{"pvalue":0.0743,"sign":1,"group":"N14: Genitourinary system diseases","label":"Prolapse and hernia of ovary and fallopian tube","text":"Phenotype: Prolapse and hernia of ovary and fallopian tube<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0743<br>N cases: 1157<br>N controls: 107564"}
{"pvalue":0.479,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other disorders of prostate","text":"Phenotype: Other disorders of prostate<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.479<br>N cases: 991<br>N controls: 119297"}
{"pvalue":0.384,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Inflammatory diseases of prostate (prostatitis)","text":"Phenotype: Inflammatory diseases of prostate (prostatitis)<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.384<br>N cases: 3760<br>N controls: 119297"}
{"pvalue":0.762,"sign":1,"group":"N14: Genitourinary system diseases","label":"Hyperplasia of prostate","text":"Phenotype: Hyperplasia of prostate<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.762<br>N cases: 30066<br>N controls: 119297"}
{"pvalue":0.766,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Acute tubulo-interstitial nephritis","text":"Phenotype: Acute tubulo-interstitial nephritis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.766<br>N cases: 23912<br>N controls: 338942"}
{"pvalue":0.065,"sign":1,"group":"N14: Genitourinary system diseases","label":"Recurrent and persistent haematuria","text":"Phenotype: Recurrent and persistent haematuria<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.065<br>N cases: 216<br>N controls: 371635"}
{"pvalue":0.443,"sign":1,"group":"N14: Genitourinary system diseases","label":"Unspecified renal colic","text":"Phenotype: Unspecified renal colic<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.443<br>N cases: 152<br>N controls: 366693"}
{"pvalue":0.245,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Renal tubulo-interstitial diseases","text":"Phenotype: Renal tubulo-interstitial diseases<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.245<br>N cases: 38335<br>N controls: 338942"}
{"pvalue":0.569,"sign":1,"group":"N14: Genitourinary system diseases","label":"Renal tubulo-interstitial disorders in diseases classified elsewhere","text":"Phenotype: Renal tubulo-interstitial disorders in diseases classified elsewhere<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.569<br>N cases: 246<br>N controls: 338942"}
{"pvalue":0.696,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Other renal tubulo-interstitial diseases","text":"Phenotype: Other renal tubulo-interstitial diseases<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.696<br>N cases: 663<br>N controls: 338942"}
{"pvalue":0.179,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Renal failure","text":"Phenotype: Renal failure<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.179<br>N cases: 14100<br>N controls: 363177"}
{"pvalue":0.802,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Unspecified kidney failure","text":"Phenotype: Unspecified kidney failure<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.802<br>N cases: 2577<br>N controls: 363177"}
{"pvalue":0.00901,"sign":1,"group":"N14: Genitourinary system diseases","label":"Salpingitis and oophoritis","text":"Phenotype: Salpingitis and oophoritis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.00901<br>N cases: 5768<br>N controls: 188295"}
{"pvalue":0.707,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Spermatocele","text":"Phenotype: Spermatocele<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.707<br>N cases: 2214<br>N controls: 119297"}
{"pvalue":0.961,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Torsion of testis","text":"Phenotype: Torsion of testis<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.961<br>N cases: 529<br>N controls: 119297"}
{"pvalue":0.852,"sign":1,"group":"N14: Genitourinary system diseases","label":"Tubulo-interstitial nephritis, not specified as acute or chronic","text":"Phenotype: Tubulo-interstitial nephritis, not specified as acute or chronic<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.852<br>N cases: 2110<br>N controls: 338942"}
{"pvalue":0.157,"sign":1,"group":"N14: Genitourinary system diseases","label":"Ulcer of vagina/vulva","text":"Phenotype: Ulcer of vagina/vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.157<br>N cases: 560<br>N controls: 188295"}
{"pvalue":0.916,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Unspecified contracted kidney","text":"Phenotype: Unspecified contracted kidney<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.916<br>N cases: 142<br>N controls: 373761"}
{"pvalue":0.183,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Urethral stricture","text":"Phenotype: Urethral stricture<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.183<br>N cases: 1597<br>N controls: 328001"}
{"pvalue":0.151,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other disorders of urethra and urinary system","text":"Phenotype: Other disorders of urethra and urinary system<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.151<br>N cases: 32905<br>N controls: 328001"}
{"pvalue":0.795,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Urethritis and urethral syndrome","text":"Phenotype: Urethritis and urethral syndrome<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.795<br>N cases: 616<br>N controls: 328001"}
{"pvalue":0.345,"sign":1,"group":"N14: Genitourinary system diseases","label":"Other diseases of urinary system","text":"Phenotype: Other diseases of urinary system<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.345<br>N cases: 49276<br>N controls: 328001"}
{"pvalue":0.137,"sign":-1,"group":"N14: Genitourinary system diseases","label":"Uterine polyps","text":"Phenotype: Uterine polyps<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.137<br>N cases: 2871<br>N controls: 107564"}
{"pvalue":0.965,"sign":1,"group":"N14: Genitourinary system diseases","label":"All dysplastic lesions of the vagina","text":"Phenotype: All dysplastic lesions of the vagina<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.965<br>N cases: 641<br>N controls: 210229"}
{"pvalue":0.445,"sign":-1,"group":"N14: Genitourinary system diseases","label":"HSIL lesion of the vagina","text":"Phenotype: HSIL lesion of the vagina<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.445<br>N cases: 335<br>N controls: 210535"}
{"pvalue":0.377,"sign":1,"group":"N14: Genitourinary system diseases","label":"LSIL lesion of the vagina","text":"Phenotype: LSIL lesion of the vagina<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.377<br>N cases: 344<br>N controls: 210526"}
{"pvalue":0.125,"sign":1,"group":"N14: Genitourinary system diseases","label":"Vaginitis/vulvovaginitis/vulvitis/abscess of vulva","text":"Phenotype: Vaginitis/vulvovaginitis/vulvitis/abscess of vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.125<br>N cases: 4648<br>N controls: 188295"}
{"pvalue":0.478,"sign":1,"group":"N14: Genitourinary system diseases","label":"All dysplastic lesions of the vulva","text":"Phenotype: All dysplastic lesions of the vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.478<br>N cases: 1118<br>N controls: 209752"}
{"pvalue":0.271,"sign":1,"group":"N14: Genitourinary system diseases","label":"HSIL lesion of the vulva","text":"Phenotype: HSIL lesion of the vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.271<br>N cases: 391<br>N controls: 210479"}
{"pvalue":0.665,"sign":1,"group":"N14: Genitourinary system diseases","label":"LSIL lesion of the vulva","text":"Phenotype: LSIL lesion of the vulva<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.665<br>N cases: 770<br>N controls: 210100"}
{"pvalue":0.0606,"sign":1,"group":"N14: Genitourinary system diseases","label":"Vulvovaginal ulceration/inflammation in other diseases","text":"Phenotype: Vulvovaginal ulceration/inflammation in other diseases<br>Category: N14: Genitourinary system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0606<br>N cases: 1494<br>N controls: 188295"}
{"pvalue":0.63,"sign":1,"group":"M13: Musculoskeletal system diseases","label":"Osteonecrosis due to drugs","text":"Phenotype: Osteonecrosis due to drugs<br>Category: M13: Musculoskeletal system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.63<br>N cases: 264<br>N controls: 377013"}
{"pvalue":0.287,"sign":1,"group":"G6: Nervous system diseases","label":"Other drug-induced secondary parkinsonism","text":"Phenotype: Other drug-induced secondary parkinsonism<br>Category: G6: Nervous system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.287<br>N cases: 234<br>N controls: 377043"}
{"pvalue":0.31,"sign":1,"group":"I9: Circulatory system diseases","label":"Phlebitis and thrombophlebitis of lower extremities, unspecified, drug-induced","text":"Phenotype: Phlebitis and thrombophlebitis of lower extremities, unspecified, drug-induced<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.31<br>N cases: 253<br>N controls: 377024"}
{"pvalue":0.252,"sign":-1,"group":"I9: Circulatory system diseases","label":"Phlebitis and thrombophlebitis of other deep vessels of lower extremities, drug-induced","text":"Phenotype: Phlebitis and thrombophlebitis of other deep vessels of lower extremities, drug-induced<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.252<br>N cases: 86<br>N controls: 377191"}
{"pvalue":0.678,"sign":1,"group":"I9: Circulatory system diseases","label":"Phlebitis and thrombophlebitis of superficial vessels of lower extremities, drug-induced","text":"Phenotype: Phlebitis and thrombophlebitis of superficial vessels of lower extremities, drug-induced<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.678<br>N cases: 83<br>N controls: 377194"}
{"pvalue":0.173,"sign":-1,"group":"L12: Skin and subcutaneous tissue diseases","label":"Psoriasis (vulgaris), strict definition","text":"Phenotype: Psoriasis (vulgaris), strict definition<br>Category: L12: Skin and subcutaneous tissue diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.173<br>N cases: 679<br>N controls: 364071"}
{"pvalue":0.6,"sign":-1,"group":"Q17: Congenital diseases","label":"Ankyloglossia","text":"Phenotype: Ankyloglossia<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.6<br>N cases: 365<br>N controls: 376912"}
{"pvalue":0.0542,"sign":-1,"group":"Q17: Congenital diseases","label":"Atrial septal defect","text":"Phenotype: Atrial septal defect<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0542<br>N cases: 1070<br>N controls: 373043"}
{"pvalue":0.34,"sign":-1,"group":"Q17: Congenital diseases","label":"Atrioventricular septal defect","text":"Phenotype: Atrioventricular septal defect<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.34<br>N cases: 108<br>N controls: 377169"}
{"pvalue":0.755,"sign":-1,"group":"Q17: Congenital diseases","label":"Balanced rearrangements and structural markers, not elsewhere classified","text":"Phenotype: Balanced rearrangements and structural markers, not elsewhere classified<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.755<br>N cases: 92<br>N controls: 376808"}
{"pvalue":0.528,"sign":-1,"group":"Q17: Congenital diseases","label":"Chromosomal abnormalities, not elsewhere classified","text":"Phenotype: Chromosomal abnormalities, not elsewhere classified<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.528<br>N cases: 469<br>N controls: 376808"}
{"pvalue":0.698,"sign":1,"group":"Q17: Congenital diseases","label":"Caries in Clefts patients , including avohilmo","text":"Phenotype: Caries in Clefts patients , including avohilmo<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.698<br>N cases: 230<br>N controls: 377047"}
{"pvalue":0.1,"sign":1,"group":"Q17: Congenital diseases","label":"Cleft hard palate NOS","text":"Phenotype: Cleft hard palate NOS<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.1<br>N cases: 125<br>N controls: 376605"}
{"pvalue":0.0776,"sign":1,"group":"Q17: Congenital diseases","label":"Cleft lip and palate","text":"Phenotype: Cleft lip and palate<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0776<br>N cases: 148<br>N controls: 376582"}
{"pvalue":0.294,"sign":1,"group":"Q17: Congenital diseases","label":"Cleft lip, lip and palate or palate","text":"Phenotype: Cleft lip, lip and palate or palate<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.294<br>N cases: 444<br>N controls: 376833"}
{"pvalue":0.742,"sign":1,"group":"Q17: Congenital diseases","label":"Cleft palate","text":"Phenotype: Cleft palate<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.742<br>N cases: 290<br>N controls: 376833"}
{"pvalue":0.0412,"sign":-1,"group":"Q17: Congenital diseases","label":"Complex cardiac defects","text":"Phenotype: Complex cardiac defects<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0412<br>N cases: 165<br>N controls: 377112"}
{"pvalue":0.231,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital deformities of feet","text":"Phenotype: Congenital deformities of feet<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.231<br>N cases: 674<br>N controls: 374712"}
{"pvalue":0.575,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital deformities of hip","text":"Phenotype: Congenital deformities of hip<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.575<br>N cases: 451<br>N controls: 374712"}
{"pvalue":0.373,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital ichthyosis","text":"Phenotype: Congenital ichthyosis<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.373<br>N cases: 89<br>N controls: 374727"}
{"pvalue":0.64,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital lens malformations","text":"Phenotype: Congenital lens malformations<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.64<br>N cases: 123<br>N controls: 375350"}
{"pvalue":0.836,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of anterior segment of eye","text":"Phenotype: Congenital malformations of anterior segment of eye<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.836<br>N cases: 222<br>N controls: 375350"}
{"pvalue":0.218,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital malformations of breast","text":"Phenotype: Congenital malformations of breast<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.218<br>N cases: 420<br>N controls: 374727"}
{"pvalue":0.926,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital malformations of cardiac chambers and connections","text":"Phenotype: Congenital malformations of cardiac chambers and connections<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.926<br>N cases: 168<br>N controls: 373043"}
{"pvalue":0.548,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of the circulatory system","text":"Phenotype: Congenital malformations of the circulatory system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.548<br>N cases: 4234<br>N controls: 373043"}
{"pvalue":0.00976,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital malformations and deformations of the musculoskeletal system","text":"Phenotype: Congenital malformations and deformations of the musculoskeletal system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00976<br>N cases: 2565<br>N controls: 374712"}
{"pvalue":0.324,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital malformations of ear causing impairment of hearing","text":"Phenotype: Congenital malformations of ear causing impairment of hearing<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.324<br>N cases: 102<br>N controls: 375350"}
{"pvalue":0.251,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of eye, ear, face and neck","text":"Phenotype: Congenital malformations of eye, ear, face and neck<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.251<br>N cases: 1927<br>N controls: 375350"}
{"pvalue":0.24,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of eyelid, lacrimal apparatus and orbit","text":"Phenotype: Congenital malformations of eyelid, lacrimal apparatus and orbit<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.24<br>N cases: 219<br>N controls: 375350"}
{"pvalue":0.571,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital malformations of gallbladder, bile ducts and liver","text":"Phenotype: Congenital malformations of gallbladder, bile ducts and liver<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.571<br>N cases: 222<br>N controls: 376152"}
{"pvalue":0.616,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of genital organs","text":"Phenotype: Congenital malformations of genital organs<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.616<br>N cases: 2867<br>N controls: 374410"}
{"pvalue":0.877,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital malformations of great arteries","text":"Phenotype: Congenital malformations of great arteries<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.877<br>N cases: 579<br>N controls: 373043"}
{"pvalue":0.138,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital malformations of the musculoskeletal system, not elsewhere classified","text":"Phenotype: Congenital malformations of the musculoskeletal system, not elsewhere classified<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.138<br>N cases: 354<br>N controls: 374712"}
{"pvalue":0.612,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of the nervous system","text":"Phenotype: Congenital malformations of the nervous system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.612<br>N cases: 563<br>N controls: 376714"}
{"pvalue":0.28,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of oesophagus","text":"Phenotype: Congenital malformations of oesophagus<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.28<br>N cases: 110<br>N controls: 376152"}
{"pvalue":0.32,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of ovaries, fallopian tubes and broad ligaments","text":"Phenotype: Congenital malformations of ovaries, fallopian tubes and broad ligaments<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.32<br>N cases: 1615<br>N controls: 374410"}
{"pvalue":0.749,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of posterior segment of eye","text":"Phenotype: Congenital malformations of posterior segment of eye<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.749<br>N cases: 134<br>N controls: 375350"}
{"pvalue":0.138,"sign":-1,"group":"Q17: Congenital diseases","label":"Congenital malformations of pulmonary and tricuspid valves","text":"Phenotype: Congenital malformations of pulmonary and tricuspid valves<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.138<br>N cases: 210<br>N controls: 373043"}
{"pvalue":0.0713,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of the respiratory system","text":"Phenotype: Congenital malformations of the respiratory system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0713<br>N cases: 454<br>N controls: 376823"}
{"pvalue":0.592,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of spine and bony thorax","text":"Phenotype: Congenital malformations of spine and bony thorax<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.592<br>N cases: 152<br>N controls: 374712"}
{"pvalue":0.264,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of trachea and bronchus","text":"Phenotype: Congenital malformations of trachea and bronchus<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.264<br>N cases: 253<br>N controls: 376823"}
{"pvalue":0.251,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of the urinary system","text":"Phenotype: Congenital malformations of the urinary system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.251<br>N cases: 1569<br>N controls: 375708"}
{"pvalue":0.867,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital malformations of uterus and cervix","text":"Phenotype: Congenital malformations of uterus and cervix<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.867<br>N cases: 574<br>N controls: 374410"}
{"pvalue":0.928,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital musculoskeletal deformities of head, face, spine and chest","text":"Phenotype: Congenital musculoskeletal deformities of head, face, spine and chest<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.928<br>N cases: 316<br>N controls: 374712"}
{"pvalue":0.55,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital obstructive defects of renal pelvis and congenital malformations of ureter","text":"Phenotype: Congenital obstructive defects of renal pelvis and congenital malformations of ureter<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.55<br>N cases: 491<br>N controls: 375708"}
{"pvalue":0.121,"sign":-1,"group":"Q17: Congenital diseases","label":"Conotruncal defects","text":"Phenotype: Conotruncal defects<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.121<br>N cases: 375<br>N controls: 376902"}
{"pvalue":0.755,"sign":-1,"group":"Q17: Congenital diseases","label":"Craniosynostosis EXCLUDE syndromes","text":"Phenotype: Craniosynostosis EXCLUDE syndromes<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.755<br>N cases: 714<br>N controls: 376563"}
{"pvalue":0.929,"sign":-1,"group":"Q17: Congenital diseases","label":"Cystic kidney disease","text":"Phenotype: Cystic kidney disease<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.929<br>N cases: 865<br>N controls: 375708"}
{"pvalue":0.949,"sign":1,"group":"Q17: Congenital diseases","label":"Down's syndrome","text":"Phenotype: Down's syndrome<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.949<br>N cases: 94<br>N controls: 376808"}
{"pvalue":0.515,"sign":-1,"group":"Q17: Congenital diseases","label":"Ehlers-Danlos syndrome","text":"Phenotype: Ehlers-Danlos syndrome<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.515<br>N cases: 236<br>N controls: 377041"}
{"pvalue":0.823,"sign":-1,"group":"Q17: Congenital diseases","label":"Hypospadias","text":"Phenotype: Hypospadias<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.823<br>N cases: 103<br>N controls: 374410"}
{"pvalue":0.571,"sign":1,"group":"Q17: Congenital diseases","label":"Congenital deformities of hip","text":"Phenotype: Congenital deformities of hip<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.571<br>N cases: 2891<br>N controls: 374386"}
{"pvalue":0.296,"sign":1,"group":"Q17: Congenital diseases","label":"Left ventricular outflow tract obstruction, narrow definition","text":"Phenotype: Left ventricular outflow tract obstruction, narrow definition<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.296<br>N cases: 1243<br>N controls: 376034"}
{"pvalue":0.197,"sign":-1,"group":"Q17: Congenital diseases","label":"Other chromosome abnormalities, not elsewhere classified","text":"Phenotype: Other chromosome abnormalities, not elsewhere classified<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.197<br>N cases: 102<br>N controls: 376808"}
{"pvalue":0.831,"sign":-1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of brain","text":"Phenotype: Other congenital malformations of brain<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.831<br>N cases: 123<br>N controls: 376714"}
{"pvalue":0.0519,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of circulatory system","text":"Phenotype: Other congenital malformations of circulatory system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.0519<br>N cases: 647<br>N controls: 373043"}
{"pvalue":0.79,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of the digestive system","text":"Phenotype: Other congenital malformations of the digestive system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.79<br>N cases: 1125<br>N controls: 376152"}
{"pvalue":0.614,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of ear","text":"Phenotype: Other congenital malformations of ear<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.614<br>N cases: 363<br>N controls: 375350"}
{"pvalue":0.488,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of face and neck","text":"Phenotype: Other congenital malformations of face and neck<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.488<br>N cases: 798<br>N controls: 375350"}
{"pvalue":0.615,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of female genitalia","text":"Phenotype: Other congenital malformations of female genitalia<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.615<br>N cases: 234<br>N controls: 374410"}
{"pvalue":0.829,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations","text":"Phenotype: Other congenital malformations<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.829<br>N cases: 2550<br>N controls: 374727"}
{"pvalue":0.465,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of heart","text":"Phenotype: Other congenital malformations of heart<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.465<br>N cases: 163<br>N controls: 373043"}
{"pvalue":0.291,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of intestine","text":"Phenotype: Other congenital malformations of intestine<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.291<br>N cases: 217<br>N controls: 376152"}
{"pvalue":0.846,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of kidney","text":"Phenotype: Other congenital malformations of kidney<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.846<br>N cases: 94<br>N controls: 375708"}
{"pvalue":0.103,"sign":-1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of limb(s)","text":"Phenotype: Other congenital malformations of limb(s)<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.103<br>N cases: 203<br>N controls: 374712"}
{"pvalue":0.583,"sign":-1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of male genital organs","text":"Phenotype: Other congenital malformations of male genital organs<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.583<br>N cases: 161<br>N controls: 374410"}
{"pvalue":0.817,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of nervous system","text":"Phenotype: Other congenital malformations of nervous system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.817<br>N cases: 239<br>N controls: 376714"}
{"pvalue":0.88,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations, not elsewhere classified","text":"Phenotype: Other congenital malformations, not elsewhere classified<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.88<br>N cases: 212<br>N controls: 374727"}
{"pvalue":0.238,"sign":-1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of peripheral vascular system","text":"Phenotype: Other congenital malformations of peripheral vascular system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.238<br>N cases: 319<br>N controls: 373043"}
{"pvalue":0.295,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of skin","text":"Phenotype: Other congenital malformations of skin<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.295<br>N cases: 1129<br>N controls: 374727"}
{"pvalue":0.934,"sign":-1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of skull and face bones","text":"Phenotype: Other congenital malformations of skull and face bones<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.934<br>N cases: 85<br>N controls: 374712"}
{"pvalue":0.886,"sign":-1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of tongue, mouth and pharynx","text":"Phenotype: Other congenital malformations of tongue, mouth and pharynx<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.886<br>N cases: 327<br>N controls: 376152"}
{"pvalue":0.625,"sign":-1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of upper alimentary tract","text":"Phenotype: Other congenital malformations of upper alimentary tract<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.625<br>N cases: 175<br>N controls: 376152"}
{"pvalue":0.262,"sign":1,"group":"Q17: Congenital diseases","label":"Other congenital malformations of urinary system","text":"Phenotype: Other congenital malformations of urinary system<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.262<br>N cases: 121<br>N controls: 375708"}
{"pvalue":0.851,"sign":-1,"group":"Q17: Congenital diseases","label":"Other congenital musculoskeletal deformities","text":"Phenotype: Other congenital musculoskeletal deformities<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.851<br>N cases: 85<br>N controls: 374712"}
{"pvalue":0.13,"sign":-1,"group":"Q17: Congenital diseases","label":"Other osteochondrodysplasias","text":"Phenotype: Other osteochondrodysplasias<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.13<br>N cases: 213<br>N controls: 374712"}
{"pvalue":0.911,"sign":1,"group":"Q17: Congenital diseases","label":"Other specified congenital malformation syndromes affecting multiple systems","text":"Phenotype: Other specified congenital malformation syndromes affecting multiple systems<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.911<br>N cases: 441<br>N controls: 374727"}
{"pvalue":0.8,"sign":-1,"group":"Q17: Congenital diseases","label":"Phakomatoses, not elsewhere classified","text":"Phenotype: Phakomatoses, not elsewhere classified<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.8<br>N cases: 284<br>N controls: 374727"}
{"pvalue":0.217,"sign":1,"group":"Q17: Congenital diseases","label":"Renal agenesis and other reduction defects of kidney","text":"Phenotype: Renal agenesis and other reduction defects of kidney<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.217<br>N cases: 129<br>N controls: 375708"}
{"pvalue":0.288,"sign":-1,"group":"Q17: Congenital diseases","label":"Right ventricular outflow tract obstruction","text":"Phenotype: Right ventricular outflow tract obstruction<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.288<br>N cases: 225<br>N controls: 377052"}
{"pvalue":0.449,"sign":-1,"group":"Q17: Congenital diseases","label":"Septal defects","text":"Phenotype: Septal defects<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.449<br>N cases: 1744<br>N controls: 375533"}
{"pvalue":0.0466,"sign":-1,"group":"Q17: Congenital diseases","label":"Undescended testicle","text":"Phenotype: Undescended testicle<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0466<br>N cases: 261<br>N controls: 374410"}
{"pvalue":0.323,"sign":1,"group":"Q17: Congenital diseases","label":"Vertebral, anorectal, cardiavascular, thracheoesophagial, renal and limb anomaly","text":"Phenotype: Vertebral, anorectal, cardiavascular, thracheoesophagial, renal and limb anomaly<br>Category: Q17: Congenital diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.323<br>N cases: 4984<br>N controls: 372293"}
{"pvalue":0.989,"sign":1,"group":"F5: Mental and behavioural disorders","label":"Use of hypnotics and sedatives","text":"Phenotype: Use of hypnotics and sedatives<br>Category: F5: Mental and behavioural disorders<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.989<br>N cases: 65814<br>N controls: 311463"}
{"pvalue":0.00771,"sign":-1,"group":"I9: Circulatory system diseases","label":"Statin medication","text":"Phenotype: Statin medication<br>Category: I9: Circulatory system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.00771<br>N cases: 127169<br>N controls: 250108"}
{"pvalue":0.638,"sign":-1,"group":"AB1: Infectious diseases","label":"Respiratory tuberculosis","text":"Phenotype: Respiratory tuberculosis<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.638<br>N cases: 1793<br>N controls: 374922"}
{"pvalue":0.677,"sign":1,"group":"K11: Digestive system diseases","label":"Temporomandibular joint disorders","text":"Phenotype: Temporomandibular joint disorders<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.677<br>N cases: 5668<br>N controls: 205355"}
{"pvalue":0.798,"sign":1,"group":"K11: Digestive system diseases","label":"Temporomandibular joint disorders, including avohilmo","text":"Phenotype: Temporomandibular joint disorders, including avohilmo<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: 1<br>p-value: 0.798<br>N cases: 13282<br>N controls: 363995"}
{"pvalue":0.105,"sign":-1,"group":"K11: Digestive system diseases","label":"Tongue abnormality","text":"Phenotype: Tongue abnormality<br>Category: K11: Digestive system diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.105<br>N cases: 1574<br>N controls: 375703"}
{"pvalue":0.0618,"sign":-1,"group":"E4: Endocrine, nutritional and metabolic diseases","label":"Vitamin deficiency","text":"Phenotype: Vitamin deficiency<br>Category: E4: Endocrine, nutritional and metabolic diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.0618<br>N cases: 1334<br>N controls: 354812"}
{"pvalue":0.567,"sign":-1,"group":"H7: Eye and adnexa diseases","label":"Wet age-related macular degeneration","text":"Phenotype: Wet age-related macular degeneration<br>Category: H7: Eye and adnexa diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.567<br>N cases: 4848<br>N controls: 252277"}
{"pvalue":0.617,"sign":-1,"group":"AB1: Infectious diseases","label":"Enteritis due to Yersinia enterocolitica","text":"Phenotype: Enteritis due to Yersinia enterocolitica<br>Category: AB1: Infectious diseases<br>rsID: rs2228145-C<br>Direction: -1<br>p-value: 0.617<br>N cases: 127<br>N controls: 371656"}