rs3761959

Parent Gene: FCRL3

Importance: 3
Less common allele: T = 46%
More common allele: C = 54%
My Genotype: Log In
Risk Allele: A, G

Disease/Trait: Graves Disease

The A allele of rs3761959 is reported to be associated with Graves Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Graves' disease.

Disease/Trait: Multiple Sclerosis

The G allele of rs3761959 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.