rs7236492

Parent Gene: NFATC1

Importance: 3
Less common allele: T = 6%
More common allele: C = 94%
My Genotype: Log In
Risk Allele: A, G

Disease/Trait: Crohn's Disease

The A allele of rs7236492 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: Inflammatory Bowel Disease

The G allele of rs7236492 is reported to be associated with Inflammatory Bowel Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Inflammatory bowel disease (EA).