rs3897478

Parent Gene: ADAM30, NOTCH2

Importance: 2
Less common allele: C = 19%
More common allele: T = 81%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Crohn's Disease

The T allele of rs3897478 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.