IL2RA, interleukin 2 receptor subunit alpha, 3559

N. diseases: 540; N. variants: 43
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12722489
rs12722489
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0010346
Disease:
Crohn Disease
C 0.800 GeneticVariation GWASCAT Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463 2010
dbSNP: rs12722489
rs12722489
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0010346
Disease:
Crohn Disease
C 0.800 GeneticVariation GWASDB Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. 21102463 2010
dbSNP: rs61839660
rs61839660
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0010346
Disease:
Crohn Disease
0.700 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908 2017
dbSNP: rs2104286
rs2104286
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0010346
Disease:
Crohn Disease
0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs3118471
rs3118471
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0010346
Disease:
Crohn Disease
0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs61839660
rs61839660
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0010346
Disease:
Crohn Disease
0.700 GeneticVariation GWASCAT Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. 26974007 2016
dbSNP: rs12722515
rs12722515
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0010346
Disease:
Crohn Disease
C 0.700 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919 2015
dbSNP: rs706778
rs706778
Entrez Id: 3559
Gene Symbol: IL2RA
IL2RA
CUI: C0010346
Disease:
Crohn Disease
T 0.700 GeneticVariation GWASCAT Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. 26301688 2015