The C (minor) allele is associated with:

  • Increased risk of gallstone disease [R].

Incomplete

rs11887534

Parent Gene: ABCG5, ABCG8

Importance: 5
Less common allele: C = 6%
More common allele: G = 94%
My Genotype: Log In
Risk Allele: C, C, C

Disease/Trait: Low Density Lipoprotein Cholesterol Measurement

The C allele of rs11887534 is reported to be associated with Low Density Lipoprotein Cholesterol Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with C-reactive protein levels or LDL-cholesterol levels (pleiotropy).

Disease/Trait: C-Reactive Protein Measurement

The C allele of rs11887534 is reported to be associated with C-reactive Protein Measurement . Your genotype was not identified for this SNP so we are unable to comment on your association with C-reactive protein levels or LDL-cholesterol levels (pleiotropy).

Disease/Trait: Gallstones

The C allele of rs11887534 is reported to be associated with Gallstones (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Gallstone disease.

Disease/Trait: Gallstones

The C allele of rs11887534 is reported to be associated with Gallstones (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Gallstone disease (EA).