rs4868644

Parent Gene: CCR4, FAF2, RNF44, TRIM71

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

Disease/Trait: Venous Thromboembolism

The T allele of rs4868644 is reported to be associated with Venous Thromboembolism (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Venous thromboembolism (SNP x SNP interaction).