The T (Minor) allele is associated with:

  • Increased risk of Crohn's Disease (R).

Incomplete

rs10210302

Parent Gene: ATG16L1, INPP5D

Importance: 2
Less common allele: T = 39%
More common allele: C = 61%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Crohn's Disease

The T allele of rs10210302 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.