Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
0.040 GeneticVariation BEFREE The H63D variant was observed in 35% and the C282Y variant as heterozygous in 5% of patients with MDS with IOL. 25841232

2015
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
0.040 GeneticVariation BEFREE The results suggest that H63D mutations may not have clinical significance in Chinese patients with MDS and AA. 20563578

2010
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
0.040 GeneticVariation BEFREE 49 patients with MM were compared to 61 patients with myelodysplastic syndrome (MDS) concerning the incidence of two genetic variants of the HFE gene (C282Y and H63D) identified with PCR-RFLP. 17001480

2006
dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
0.040 GeneticVariation BEFREE Genotypic testing of nonselected patients with the myelodysplastic syndrome (MDS) for the C282Y and H63D mutations of the HFE gene responsible for hereditary hemochromatosis revealed a significantly increased frequency of these mutations when compared to healthy blood donors reflecting the average population. 12624489

2003