Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Correlation between the 677C>T polymorphism in the methylene tetrahydrofolate reductase gene and serum homocysteine levels in coronary heart disease. 27051002 2016
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Methylenetetrahydrofolate reductase C677T polymorphism is associated with increased risk of coronary artery disease in young South African Indians. 26095803 2015
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE The association of MTHFR C677T gene variants and lipid profiles or body mass index in patients with diabetic and nondiabetic coronary heart disease. 24218123 2013
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Methylenetetrahydrofolate reductase C677T gene polymorphism and coronary artery disease in a Chinese Han population: a meta-analysis. 22146089 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Role of homocysteine & MTHFR C677T gene polymorphism as risk factors for coronary artery disease in young Indians. 22664498 2012
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Detection of C677T mutation of MTHFR in subject with coronary heart disease by hairpin probe with enzymatic color on microarray. 21802936 2011
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE The C677T polymorphism of 5,10 methylenetetrahydrofolate reductase (MTHFR) gene has been associated with hypertension and coronary artery disease in several populations worldwide, but results are still controversial. 20637366 2010
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE High plasma homocysteine is associated with the risk of coronary artery disease independent of methylenetetrahydrofolate reductase 677C-->T genotypes. 18586656 2008
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE The C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene is associated with early onset of coronary artery disease in some populations with certain ethnic backgrounds. 18751630 2008
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Plasma homocysteine levels & 677C-->T methylenetetrahydrofolate reductase gene polymorphism in patients with coronary artery disease of different severity. 18403793 2008
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Dynamic regulation of MTHFR mRNA expression and C677T genotype modulate mortality in coronary artery disease patients after revascularization. 17604826 2007
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Sex-specific effect of the thermolabile C677T mutation in the methylenetetrahydrofolate reductase gene on angiographically assessed coronary artery disease in Brazilians. 18075008 2007
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Gene--nutrition interactions in coronary artery disease: correlation between the MTHFR C677T polymorphism and folate and homocysteine status in a Korean population. 15935452 2006
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE C677T mutation of methylenetetrahydrofolate reductase gene and serum homocysteine levels in Turkish patients with coronary artery disease. 15648053 2006
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Recent studies have shown that a common mutation (nucleotide 677 C-->T) in the methylenetetrahydrofolate reductase (MTHFR) gene may contribute to a mild rise in plasma homocysteine levels and increase the incidence of coronary artery disease. 16489563 2006
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE The oxidative modification of low-density lipoprotein (LDL) has been suggested to be a key element in atherogenesis, while methylenetetrahydrofolate reductase (MTHFR) C677T mutation has been associated with the development of coronary heart disease. 16487909 2006
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE The objective of our study is to evaluate the single locus and combined effects of three different genetic polymorphisms (methylenetetrahydrofolate reductase C677T polymorphism, plasminogen activator inhibitor 4G/5G polymorphism, and endothelial nitric oxide synthase 3-27 base pairs repeat polymorphism) on the presence and extent of coronary artery disease in patients with early-onset coronary artery disease. 16845248 2006
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE No strong evidence exists to support an association of the MTHFR 677 C-->T polymorphism and coronary heart disease in Europe, North America, or Australia. 16216822 2005
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE One putative determinant of PAD is the 677C>T polymorphism in the gene encoding methylenetetrahydrofolate reductase (MTHFR), which has previously been found to associate with various diabetic complications including retinopathy, nephropathy, atherosclerosis and coronary heart disease. 16274479 2005
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE We studied several single nucleotide polymorphisms (SNP) in Hcy-regulating genes [methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C; methionine synthase (MS) A2756G; methionine synthase reductase (MTRR) A66G] in relation to total plasma Hcy levels, transplant coronary artery disease and thromboembolic episodes in 84 heart transplant patients, and we compared the incidence of these polymorphisms with those in a healthy adult controls. 15612980 2005
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease. 15353918 2004
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE The 5,10-methylenetetrahydrofolate reductase gene (MTHFR) 677C-->T polymorphism modifies the risk of coronary artery disease and colon cancer and is related to plasma concentrations of total homocysteine (tHcy). 15447919 2004
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Prevalence and role of methylenetetrahydrofolate reductase 677 C-->T and 1298 A-->C polymorphisms in coronary artery disease in Arabs. 14521457 2003
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE We investigated the influence of elevated homocysteine plasma levels and 2 polymorphisms, 677C/T and 1298A/C, of the methylenetetrahydrofolate reductase (MTHFR) gene on the risk of restenosis after stenting in patients with symptomatic coronary artery disease. 14604831 2003
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.100 GeneticVariation BEFREE Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease. 12522558 2003