present in Gene: MYPN
present in Chromosome: 10
Position on Chromosome: 68210229
Alleles of this Variant: C/T
rs10998022 in
MYPN 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.
rs10998022 in
MYPN 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.