Variant: rs6598902

present in Gene: STX12 present in Chromosome: 1 Position on Chromosome: 27779198 Alleles of this Variant: T/C

rs6598902 in STX12 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.

rs6598902 in STX12 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.