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.