Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.070 GeneticVariation BEFREE In addition, the results of our case-control study indicated that rs1800562 and rs1800730 were monomorphic, and that rs1799945 and rs9366637 were not associated with CHD in Han Chinese. 23792061 2013
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.070 GeneticVariation BEFREE Previous studies have suggested a positive association of coronary heart disease risk and both serum ferritin concentrations and C282Y heterozygosity. 20031565 2009
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.070 GeneticVariation BEFREE After full adjustment, the odds ratio for coronary heart disease was 1.12 (95% CI, 0.92 to 1.37) for subjects with the compound heterozygous (C282Y/H63D) genotype relative to those with the wild-type/wild-type genotype. 20031541 2008
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.070 GeneticVariation BEFREE Compared with non-carriers, those that carried the C282Y allele were not at increased risk for CHD (HR = 1.25, 95% CI = 0.74-2.09). 16968463 2006
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.070 GeneticVariation BEFREE Haemochromatosis-causing mutations C282Y and H63D are not risk factors for coronary artery disease in Caucasians with type 2 diabetes. 15222129 2004
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.070 GeneticVariation BEFREE We examined the relation between two HFE mutations (C282Y and H63D), indicators of iron homeostasis, and the prevalence of coronary heart disease in a large population of white adults. 12427496 2002
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
0.070 GeneticVariation BEFREE Our prospective findings suggest that individuals carrying the HFE C282Y mutation may be at increased risk of CHD. 11257277 2001