Variant: rs16824658

present in Gene: HMCN1 present in Chromosome: 1 Position on Chromosome: 185895380 Alleles of this Variant: A/G

rs16824658 in HMCN1 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.

rs16824658 in HMCN1 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.