Variant: rs17241442

present in Gene: TNC;DELEC1 present in Chromosome: 9 Position on Chromosome: 115062806 Alleles of this Variant: G/A

rs17241442 in TNC;DELEC1 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.

rs17241442 in TNC;DELEC1 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.