Variant: rs41360247 

    present in Gene: ABCG8;LOC102725159
    present in Chromosome: 2
    Position on Chromosome: 43846517
    Alleles of this Variant: T/C

rs41360247 in ABCG8;LOC102725159 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.

rs41360247 in ABCG8;LOC102725159 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.