The SNP is associated with the following:

  • Crohn's disease (P=1.00*10-8) (R).

rs10889676

Parent Gene: C1ORF141, DOCK7, IL23R

Importance: 5
Less common allele: A = 39%
More common allele: C = 61%
My Genotype: Log In
Risk Allele:

Disease/Trait: Crohn's Disease

rs10889676 is associated with Crohn's Disease (R) . It is reported to increased association with Crohn's disease. No specific risk allele was identified in the study.

Disease/Trait: Crohn's Disease

rs10889676 is associated with Crohn's Disease (R) . It is reported to increased association with Crohn's disease. No specific risk allele was identified in the study.