|
rs429358
|
|
|
0.020 |
GeneticVariation |
BEFREE |
<b>Aim:</b> To explore the association of APOE polymorphism (rs7412:526C>T and rs429358:388T>C) with glucose, lipid and serum uric acid (UA) metabolism in patients with hypertension or coronary heart disease (CHD).
|
31559922 |
2019 |
|
rs6882076
|
|
|
0.010 |
GeneticVariation |
BEFREE |
<b>Conclusions</b>: The results of the present study suggest that the <i>TIMD4</i> rs6882076 SNP is associated with decreased risk of CHD and IS in our study population.
|
31337960 |
2019 |
|
rs7041
|
|
|
0.030 |
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 |
|
rs9982601
|
|
|
0.810 |
GeneticVariation |
BEFREE |
<i>Background</i>.The coronary heart disease (CHD) risk locus on 21q22 (lead SNP rs9982601) lies within a "gene desert."
|
28458444 |
2017 |
|
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 |
|
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 |
|
rs1805017
|
|
|
0.040 |
GeneticVariation |
BEFREE |
14 association studies focusing on three polymorphisms (A379V, V279F and R92H) in PLA2G7 gene and risk of CHD were included in meta-analysis, covering a total of 8,280 cases and 5,656 controls.
|
20926117 |
2010 |
|
rs1800588
|
|
|
0.720 |
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 |
|
rs1541861
|
|
|
0.010 |
GeneticVariation |
BEFREE |
CHD risk was significantly higher among men with the variant allele at the rs1541861 locus (intron 8 A/C) than men without it (adjusted odds ratio 1.5 [95% confidence interval 1.1-2.1]).
|
16804086 |
2006 |
|
rs5443
|
|
|
0.020 |
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 |
|
rs699
|
|
|
0.100 |
GeneticVariation |
BEFREE |
M235T and T174M variants do not contribute to the increased risk of CHD or hypertension in the Indian population.
|
12938141 |
2003 |
|
rs1267969615
|
|
|
0.080 |
GeneticVariation |
BEFREE |
M235T and T174M variants do not contribute to the increased risk of CHD or hypertension in the Indian population.
|
12938141 |
2003 |
|
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
|
|
|
0.720 |
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 |
|
rs7025486
|
|
|
0.020 |
GeneticVariation |
BEFREE |
rs7025486 was genotyped in 1386 CHD cases and 3532 controls and was associated with CHD [odds ratio (OR) of 1.16, 95% confidence interval (CI) 1.05-1.29, P= 0.003].
|
21444365 |
2012 |
|
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
|
|
|
0.830 |
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 |
|
rs174547
|
|
|
0.830 |
GeneticVariation |
BEFREE |
rs174547 in FADS1 may contribute to the susceptibility of CHD by altering HDL-C and TG levels in Chinese individuals.
|
22490578 |
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 |