TF, transferrin, 7018

N. diseases: 47; N. variants: 70
Disease: Transferrin measurement ×
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8177179
rs8177179
Entrez Id: 7018;100129696
Gene Symbol: TF;INHCAP
TF;INHCAP
CUI: C0202105
Disease:
Transferrin measurement 		A 0.700 GeneticVariation GWASCAT Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. 25352340 2014