rs4613763

Parent Gene: LOC105374736, LOC105374737

Importance: 3
Less common allele: C = 9%
More common allele: T = 91%
My Genotype: Log In
Risk Allele: C, G

Disease/Trait: Crohn's Disease

The C allele of rs4613763 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: Multiple Sclerosis

The G allele of rs4613763 is reported to be associated with Multiple Sclerosis (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Multiple sclerosis.