Variant: rs8177179 

    present in Gene: INHCAP;TF
    present in Chromosome: 3
    Position on Chromosome: 133744613
    Alleles of this Variant: G/A

rs8177179 in INHCAP;TF gene and Serum transferrin measurement PMID 25352340 2014 Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.

rs8177179 in INHCAP;TF gene and Transferrin measurement PMID 25352340 2014 Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.