Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Further subgroup analyses according to ethnicity of participants revealed that the rs1799983 and rs2070744 polymorphisms were significantly associated with the risk of coronary artery disease in both Caucasians and Asians, whereas the rs869109213 polymorphism was only associated with the risk of coronary artery disease in Caucasians. 30789045

2019

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE In addition, we also found that the rs1799983 polymorphism was significantly associated with the susceptibility to peripheral artery disease, whereas the rs2070744 polymorphism was significantly associated with the susceptibility to coronary artery disease in DM patients. 30140993

2018

dbSNP: rs662
rs662
0.100 GeneticVariation BEFREE Association between the PON1 Q192R polymorphism and coronary heart disease in Chinese: A meta-analysis. 29952962

2018

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Association Patterns of Endothelial Nitric Oxide Synthase Gene (NOS3) Variant Glu298Asp with Blood Pressure and Serum Lipid Levels in Subjects with Coronary Artery Disease from Pakistan. 28620990

2017

dbSNP: rs1217691063
rs1217691063
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

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Genetic polymorphisms of eNOS (-786T/C, Intron 4b/4a & 894G/T) and its association with asymptomatic first degree relatives of coronary heart disease patients. 27613099

2016

dbSNP: rs662
rs662
0.100 GeneticVariation BEFREE The activity of PON1 is decreased in patients with coronary artery disease, myocardial infarction or chronic kidney disease. rs662 and rs854560 are single nucleotide polymorphisms (SNPs) associated with PON1 activity and 10-year cardiovascular mortality of patients with stable coronary artery disease. 25155309

2016

dbSNP: rs699
rs699
AGT
0.100 GeneticVariation BEFREE Relationship of the rs1799752 polymorphism of the angiotensin-converting enzyme gene and the rs699 polymorphism of the angiotensinogen gene to the process of in-stent restenosis in a population of Polish patients with stable coronary artery disease. 27162064

2016

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Methylenetetrahydrofolate reductase C677T polymorphism is associated with increased risk of coronary artery disease in young South African Indians. 26095803

2015

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE On the basis of present results, it can be concluded that rs1799983 is strongly associated with coronary artery disease in our population and TT genotype of this polymorphism enhanced the risk of coronary artery disease in Pakistani population. 25057159

2015

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE AF patients with rs1799983 variants were more likely to have coronary artery disease or stroke than those without genetic variant at this gene (31.0% vs. 17.3%, p=0.004). 26256966

2015

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Effects of eNOS rs1799983 and ACE rs4646994 polymorphisms on the therapeutic efficacy of salvianolate injection in Chinese patients with coronary heart disease. 24827774

2014

dbSNP: rs662
rs662
0.100 GeneticVariation BEFREE Association between PON1 rs662 polymorphism and coronary artery disease. 24918121

2014

dbSNP: rs1217691063
rs1217691063
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

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Association between the endothelial nitric oxide synthase gene Glu298Asp polymorphism and coronary heart disease: a meta‑analysis of 39 case‑control studies. 23443250

2013

dbSNP: rs662
rs662
0.100 GeneticVariation BEFREE Association of paraoxonase1 gene Q192R polymorphism and apolipoprotein B in Asian Indian women with coronary artery disease risk. 23171143

2013

dbSNP: rs662
rs662
0.100 GeneticVariation BEFREE The Q192R polymorphism of the paraoxonase 1 gene is a risk factor for coronary artery disease in Saudi subjects. 23625196

2013

dbSNP: rs699
rs699
AGT
0.100 GeneticVariation BEFREE AGT gene polymorphisms (M235T, T174M) are associated with coronary heart disease in a Chinese population. 22791700

2013

dbSNP: rs699
rs699
AGT
0.100 GeneticVariation BEFREE The M235T single nucleotide polymorphism in the angiotensinogen gene is associated with coronary artery calcium in patients with a family history of coronary artery disease. 23137822

2013

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Methylenetetrahydrofolate reductase C677T gene polymorphism and coronary artery disease in a Chinese Han population: a meta-analysis. 22146089

2012

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Role of homocysteine & MTHFR C677T gene polymorphism as risk factors for coronary artery disease in young Indians. 22664498

2012

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE Association of endothelial nitric oxide synthase gene variant (G894T) with coronary artery disease in Western Iran. 21602253

2012

dbSNP: rs1799983
rs1799983
0.100 GeneticVariation BEFREE The G894T polymorphism on endothelial nitric oxide synthase gene is associated with increased coronary heart disease among Asia population: evidence from a Meta analysis. 22417945

2012

dbSNP: rs699
rs699
AGT
0.100 GeneticVariation BEFREE Angiotensinogen gene M235T polymorphism and risk of coronary artery disease: a meta-analysis. 22842872

2012

dbSNP: rs1217691063
rs1217691063
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