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.