The SNP is associated with the following:

  • Crohn's disease (P=1.00*10-8) (R)
  • Psoriasis (P=3.00*10-8) (R)

Incomplete

rs2201841

Parent Gene: C1ORF141, IL23R

Importance: 5
Less common allele: G = 40%
More common allele: A = 60%
My Genotype: Log In
Risk Allele: G, C

Disease/Trait: Crohn's Disease

rs2201841 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

rs2201841 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: Psoriasis

The G allele of rs2201841 is reported to be associated with Psoriasis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Psoriasis.

Disease/Trait: Ulcerative Colitis

The C allele of rs2201841 is reported to be associated with Ulcerative Colitis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Ulcerative colitis.