Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs750609759
rs750609759
TFR2
C 0.700 GeneticVariation CLINVAR Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3. 26029709

2015
dbSNP: rs750609759
rs750609759
TFR2
C 0.700 GeneticVariation CLINVAR Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observations. 23600741

2013