rs16967103

Parent Gene: RASGRP1

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

Disease/Trait: Crohn's Disease

The C allele of rs16967103 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: Inflammatory Bowel Disease

The G allele of rs16967103 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).

Disease/Trait: Crohn's Disease

rs16967103 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.