rs9988642

Parent Gene: C1ORF141, IL23R

Importance: 5
Less common allele: C = 12%
More common allele: T = 88%
My Genotype: Log In
Risk Allele: T

Disease/Trait: Psoriasis Vulgaris

The T allele of rs9988642 is reported to be associated with Psoriasis Vulgaris . Your genotype was not identified for this SNP so we are unable to comment on your association with Psoriasis vulgaris.

Disease/Trait: Crohn's Disease

rs9988642 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

rs9988642 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.