|
rs7041
|
|
|
0.020 |
GeneticVariation |
BEFREE |
<b>Objectives</b>: The vitamin D binding protein encoded by the <i>GC</i> gene contains two single nucleotide polymorphisms (rs4588 and rs7041) that have been associated with disease outcome, these include periodontitis coronary heart disease and hypertension.
|
31559882 |
2019 |
|
rs8259
|
|
|
0.010 |
GeneticVariation |
BEFREE |
<i>BSG</i> rs8259 TT genotype was associated with a decreased risk of CHF (OR = 0.83, 95% CI = 0.72-0.96, <i>p</i> = 0.010), especially in patients with hypertension (OR = 0.80, 95% CI = 0.68-0.95, <i>p</i> = 0.011) and coronary heart disease (OR = 0.81, 95% CI = 0.69-0.96, <i>p</i> = 0.013) after adjustment for multiple cardiovascular risk factors.
|
28230811 |
2017 |
|
rs6882076
|
|
|
0.010 |
GeneticVariation |
BEFREE |
<i>TIMD4</i> rs6882076 SNP Is Associated with Decreased Levels of Triglycerides and the Risk of Coronary Heart Disease and Ischemic Stroke.
|
31337960 |
2019 |
|
rs4646903
|
|
|
0.010 |
GeneticVariation |
BEFREE |
1.The CYP1A1 T6235C polymorphism (rs4646903) gene polymorphism has been linked to the development of coronary heart disease and cigarette smoking-related lung cancer.
|
19650794 |
2010 |
|
rs1800588
|
|
|
0.020 |
GeneticVariation |
BEFREE |
557 men aged 45-74 with stable coronary artery disease and 560 paired controls were genotyped for rs1800588.
|
23874450 |
2013 |
|
rs662
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Coronary artery disease risk in Chinese type 2 diabetics: is there a role for paraxonase 1 gene (Q192R) polymorphism?
|
11375798 |
2001 |
|
rs5443
|
|
|
0.010 |
GeneticVariation |
BEFREE |
C825T polymorphism in the G protein beta3 subunit gene (GNB3) has been associated with arterial hypertension, coronary artery disease and myocardial infarction.
|
10704626 |
2000 |
|
rs6020
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Arg485Lys polymorphism of factor V increases the risk of coronary artery disease in a Chinese population.
|
11776127 |
2000 |
|
rs1799983
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Glu298-->Asp polymorphism of the eNOS gene appears to be associated with the presence, extent, and severity of angiographically assessed coronary artery disease.
|
12010932 |
2002 |
|
rs16139
|
|
|
0.050 |
GeneticVariation |
BEFREE |
Leucine 7 to proline 7 polymorphism in the preproneuropeptide Y is associated with proteinuria, coronary heart disease, and glycemic control in type 1 diabetic patients.
|
14747236 |
2004 |
|
rs1217691063
|
|
|
0.100 |
GeneticVariation |
BEFREE |
C677T mutation of methylenetetrahydrofolate reductase gene and serum homocysteine levels in Turkish patients with coronary artery disease.
|
15648053 |
2006 |
|
rs1199475313
|
|
|
0.010 |
GeneticVariation |
BEFREE |
T64A polymorphism in beta3-adrenergic receptor gene (ADRB3) and coronary heart disease: a case-cohort study and meta-analysis.
|
18088254 |
2008 |
|
rs7903146
|
|
|
0.020 |
GeneticVariation |
BEFREE |
rs7903146 T allele is associated with diabetes and, in non-diabetic individuals, with a higher prevalence and severity of coronary artery disease and cardiovascular events. name of registry site (see list below), registration number, trial registration URL in brackets.
|
19924244 |
2009 |
|
rs1799983
|
|
|
0.100 |
GeneticVariation |
BEFREE |
G894T polymorphism of eNOS gene was not associated with foot ulcer and diabetic complications, except in the presence of atherosclerotic heart disease.
|
20642368 |
2010 |
|
rs1799983
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Glu298Asp polymorphism of the endothelial nitric oxide synthase (eNOS) gene (NOS3) has been characterized as a risk factor of hypertension and coronary artery disease.
|
21816783 |
2011 |
|
rs1049353
|
|
|
0.010 |
GeneticVariation |
BEFREE |
G1359A polymorphism in the cannabinoid receptor-1 gene is associated with the presence of coronary artery disease in patients with type 2 diabetes.
|
22138970 |
2012 |
|
rs2943634
|
|
|
0.010 |
GeneticVariation |
BEFREE |
rs2943634 C/A single nucleotide polymorphism (SNP), located in a non coding region of chromosome 2q36.3, has been associated with coronary artery disease in two genome wide association studies.
|
22207032 |
2012 |
|
rs1181860747
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Gly1057Asp polymorphism of insulin receptor substrate-2 is associated with coronary artery disease in the Taiwanese population.
|
23216712 |
2012 |
|
rs1805097
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Gly1057Asp polymorphism of insulin receptor substrate-2 is associated with coronary artery disease in the Taiwanese population.
|
23216712 |
2012 |
|
rs25487
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Arg399Gln polymorphism of X-ray repair cross-complementing group 1 gene is associated with angiographically documented coronary artery disease in South Indian type 2 diabetic patients.
|
23360319 |
2013 |
|
rs20455
|
|
|
0.090 |
GeneticVariation |
BEFREE |
Trp 719Arg have an effect on development of Coronary Heart Disease but it is very useful for statin therapy.
|
26443250 |
2015 |
|
rs72653706
|
|
|
0.050 |
GeneticVariation |
BEFREE |
A 16-year-old survivor of acute myocardial infarction with 3-vessel coronary artery disease exhibited compound heterozygosity for the well-known nonsense mutation (c.3421C>T; R1141X) in exon 24 and a novel missense mutation (c.3662G>A; R1221H) in exon 26 of the ABCC6 gene.
|
16854481 |
2007 |
|
rs63751001
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A 16-year-old survivor of acute myocardial infarction with 3-vessel coronary artery disease exhibited compound heterozygosity for the well-known nonsense mutation (c.3421C>T; R1141X) in exon 24 and a novel missense mutation (c.3662G>A; R1221H) in exon 26 of the ABCC6 gene.
|
16854481 |
2007 |
|
rs6903956
|
|
|
0.030 |
GeneticVariation |
BEFREE |
A coronary artery disease-associated SNP rs6903956 contributed to asymptomatic hyperuricemia susceptibility in Han Chinese.
|
25928384 |
2015 |
|
rs974819
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A case-control study provides evidence of association for a common SNP rs974819 in PDGFD to coronary heart disease and suggests a sex-dependent effect.
|
22704460 |
2012 |