Variant: rs9906298

present in Gene: CA10 present in Chromosome: 17 Position on Chromosome: 51702890 Alleles of this Variant: T/C

rs9906298 in CA10 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.

rs9906298 in CA10 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.