rs7746082

Parent Gene: PRDM1

Importance: 3
Less common allele: C = 11%
More common allele: G = 89%
My Genotype: Log In
Risk Allele: C, C, C

Disease/Trait: Crohn's Disease

The C allele of rs7746082 is reported to be associated with Crohn's Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Crohn's disease.

Disease/Trait: Ulcerative Colitis

The C allele of rs7746082 is reported to be associated with Ulcerative Colitis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Ulcerative colitis (EA).

Disease/Trait: Crohn's Disease

The C allele of rs7746082 is reported to be associated with Crohn's Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Crohn's disease (EA).

Disease/Trait: Crohn's Disease

rs7746082 is associated with Crohn's Disease (R) . It is reported to association with Crohn's disease. No specific risk allele was identified in the study.

Disease/Trait: Inflammatory Bowel Disease

rs7746082 is associated with Inflammatory Bowel Disease (R) . It is reported to association with Inflammatory bowel disease. No specific risk allele was identified in the study.