rs3091338

Parent Gene: CSF2, IL3

Importance: 3
Less common allele: T = 16%
More common allele: C = 84%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Crohn's Disease

The T allele of rs3091338 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.