TF, transferrin, 7018

N. diseases: 168; N. variants: 74
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders
0.100 GeneticVariation group GWASCAT Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. 25457201 2015