rs10479002

Parent Gene: SLC22A4

Importance: 3
Less common allele: G = 2%
More common allele: C = 98%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Fibrinogen Measurement

The C allele of rs10479002 is reported to be associated with Fibrinogen Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Fibrinogen.