rs3811647, TF

N. diseases: 15
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Iron Metabolism Disorders
CUI: C0012715
Disease: Iron Metabolism Disorders
0.700 GeneticVariation GWASCAT Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. 25457201 2015