TFR2, transferrin receptor 2, 7036

N. diseases: 92; N. variants: 50
Disease: Hereditary hemochromatosis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1426704853
rs1426704853
Entrez Id: 7036
Gene Symbol: TFR2
TFR2
CUI: C0392514
Disease:
Hereditary hemochromatosis 		A 0.700 CausalMutation CLINVAR