Variant: rs121917848 

    present in Gene: SLC10A2
    present in Chromosome: 13
    Position on Chromosome: 103051290
    Alleles of this Variant: A/G

rs121917848 in SLC10A2 gene and Bile Acid Malabsorption, Primary PMID 9109432 1997 Primary bile acid malabsorption caused by mutations in the ileal sodium-dependent bile acid transporter gene (SLC10A2).