Variant: rs1475029 

    present in Gene: LOC729296;MIR646HG
    present in Chromosome: 20
    Position on Chromosome: 60093953
    Alleles of this Variant: A/G

rs1475029 in LOC729296;MIR646HG 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.

rs1475029 in LOC729296;MIR646HG 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.