Variant: rs121918681 

    present in Gene: INHCAP;TF
    present in Chromosome: 3
    Position on Chromosome: 133753607
    Alleles of this Variant: G/A

rs121918681 in INHCAP;TF gene and Congenital atransferrinemia PMID 15466165 2004 Molecular characterization of a third case of human atransferrinemia.

PMID 11110675 2000 Molecular characterization of a case of atransferrinemia.