Variant: rs11186149

present in Gene: SH2D4B present in Chromosome: 10 Position on Chromosome: 80580951 Alleles of this Variant: T/C

rs11186149 in SH2D4B 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.

rs11186149 in SH2D4B 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.