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: rs786204108
rs786204108
Entrez Id: 7036
Gene Symbol: TFR2
TFR2
CUI: C0392514
Disease:
Hereditary hemochromatosis 		G 0.700 GeneticVariation CLINVAR Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype. 26408288 2015
dbSNP: rs786204108
rs786204108
Entrez Id: 7036
Gene Symbol: TFR2
TFR2
CUI: C0392514
Disease:
Hereditary hemochromatosis 		G 0.700 GeneticVariation CLINVAR Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observations. 23600741 2013