rs148685782

Parent Gene: FGG

Importance: 5
Less common allele: C = 0%
More common allele: G = 100%
My Genotype: Log In
Risk Allele: C

Disease/Trait: Fibrinogen Measurement

The C allele of rs148685782 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 levels.