rs3811647, TF

N. diseases: 15
Disease: Hereditary hemochromatosis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
0.710 GeneticVariation BEFREE Because these two outcomes were clearly associated with the biochemical and clinical expression of the disease, an indirect link between the rs3811647 polymorphism and the phenotypic presentation of HFE-HH is likely. 25457201 2015
Hereditary hemochromatosis
CUI: C0392514
Disease: Hereditary hemochromatosis
0.710 GeneticVariation GWASCAT Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. 25457201 2015