Variant: rs135851

present in Gene: C22orf34 present in Chromosome: 22 Position on Chromosome: 49583909 Alleles of this Variant: A/C

rs135851 in C22orf34 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.

rs135851 in C22orf34 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.