Variant: rs11887534 

    present in Gene: ABCG5;ABCG8
    present in Chromosome: 2
    Position on Chromosome: 43839108
    Alleles of this Variant: G/A;C

rs11887534 in ABCG5;ABCG8 gene and Biliary calculi PMID 30692554 2019 Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry.

PMID 17632509 2007 A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

PMID 27094239 2016 Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies.

PMID 30504769 2018 Genome-wide association meta-analysis yields 20 loci associated with gallstone disease.

rs11887534 in ABCG5;ABCG8 gene and C-reactive protein measurement PMID 27286809 2016 Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.

rs11887534 in ABCG5;ABCG8 gene and Cholecystolithiasis PMID 17632509 2007 A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

rs11887534 in ABCG5;ABCG8 gene and Cholelithiasis PMID 17632509 2007 A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

rs11887534 in ABCG5;ABCG8 gene and Low density lipoprotein cholesterol measurement PMID 27286809 2016 Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.