Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs786204108
rs786204108
TFR2
G 0.700 GeneticVariation CLINVAR Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype. 26408288

2015
dbSNP: rs786204108
rs786204108
TFR2
G 0.700 GeneticVariation CLINVAR Variable age of onset and clinical severity in transferrin receptor 2 related haemochromatosis: novel observations. 23600741

2013