Variant: rs9872999 

    present in Gene: TF;INHCAP
    present in Chromosome: 3
    Position on Chromosome: 133738670
    Alleles of this Variant: C/G;T

rs9872999 in TF;INHCAP gene and Iron binding capacity total measurement PMID 25224454 2015 Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans.

rs9872999 in TF;INHCAP gene and Total iron binding capacity function PMID 25224454 2015 Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans.