rs1656404

Parent Gene: ECEL1, PRSS56

Importance: 2
Less common allele: A = 15%
More common allele: G = 85%
My Genotype: Log In
Risk Allele: A

Disease/Trait: Abnormality Of Refraction

The A allele of rs1656404 is reported to be associated with Abnormality Of Refraction (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Refractive error.