Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.500 GeneticVariation disease BEFREE Association between the polymorphism of estrogen receptor α and coronary artery disease in a Chinese population. 22284250 2012
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.500 Biomarker disease BEFREE Collectively, these data revealed that Catalpol inhibited apoptosis and oxidative stress in glucose-deprived H9c2 cell through promoting cell mitophagy and modulating estrogen receptor, supporting the notion that Catalpol could be a novel drug candidate against myocardial ischemia for the treatment of cardiovascular diseases. 28292026 2017
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.500 Biomarker disease CTD_human Premature coronary artery disease associated with a disruptive mutation in the estrogen receptor gene in a man. 9396482 1997
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.500 GeneticVariation disease BEFREE Gender-specific effect of estrogen receptor-1 gene polymorphisms in coronary artery disease and its angiographic severity in Chinese population. 18582450 2008
Entrez Id: 2099
Gene Symbol: ESR1
ESR1
0.500 Biomarker disease BEFREE To test whether estrogen receptor polymorphisms modify the effects of postmenopausal hormone therapy on biomarkers and on risk of coronary heart disease events, stroke, or venous thromboembolism. 21106950 2011
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.420 GeneticVariation disease BEFREE A female subject with each mutation was symptomatic with coronary atherosclerosis: a 5-year-old ABCG8 S107X homozygote and a 75-year-old ABCG5 exon 3 I/D homozygote; these represent the extreme ends of the spectrum of vascular involvement in sitosterolemia. 15375183 2004
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.420 Biomarker disease CTD_human Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters. 11099417 2000
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.420 GeneticVariation disease BEFREE Effect of genetic variant (rs11887534) in ABCG8 gene in coronary artery disease and response to atorvastatin therapy. 20592455 2010
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8
0.420 Biomarker disease HPO
Entrez Id: 64240
Gene Symbol: ABCG5
ABCG5
0.410 Biomarker disease CTD_human Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters. 11099417 2000
Entrez Id: 64240
Gene Symbol: ABCG5
ABCG5
0.410 Biomarker disease CTD_human Identification of a gene, ABCG5, important in the regulation of dietary cholesterol absorption. 11138003 2001
Entrez Id: 64240
Gene Symbol: ABCG5
ABCG5
0.410 GeneticVariation disease BEFREE ABCG5/8 variants are associated with susceptibility to coronary heart disease. 24691589 2014
Entrez Id: 64240
Gene Symbol: ABCG5
ABCG5
0.410 Biomarker disease HPO
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.400 GeneticVariation disease 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
Entrez Id: 7099
Gene Symbol: TLR4
TLR4
0.400 GeneticVariation disease BEFREE Promoter Polymorphism of Toll-Like Receptor 4 is Associated with a Decreased Risk of Coronary Artery Disease: A Case-Control Study in the Chinese Han Population. 28092654 2017
Entrez Id: 5444
Gene Symbol: PON1
PON1
0.400 GeneticVariation disease BEFREE Association between the PON1 Q192R polymorphism and coronary heart disease in Chinese: A meta-analysis. 29952962 2018
Entrez Id: 7099
Gene Symbol: TLR4
TLR4
0.400 GeneticVariation disease BEFREE The effect of genetic polymorphisms of TLR2 and TLR4 in Turkish patients with coronary artery disease. 25542811 2015
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.400 AlteredExpression disease BEFREE Shear stress insensitivity of endothelial nitric oxide synthase expression as a genetic risk factor for coronary heart disease. 15375006 2004
Entrez Id: 1401
Gene Symbol: CRP
CRP
0.400 GeneticVariation disease BEFREE Several pro-inflammatory cytokines, such as the C-reactive protein (CRP), tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) have been described as independent risk factors for coronary heart disease and promoters of atherogenesis. 31157268 2019
Entrez Id: 335
Gene Symbol: APOA1
APOA1
0.400 AlteredExpression disease BEFREE The proinflammatory enzyme myeloperoxidase induces both oxidative modification and nitrosylation of specific residues on plasma and arterial apolipoprotein A-I to render HDL dysfunctional, which results in impaired ABCA1 macrophage transport, the activation of inflammatory pathways, and an increased risk of coronary artery disease. 26323267 2016
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.400 GeneticVariation disease BEFREE Several studies have shown that the T-786C polymorphism in 5'-flanking region of the endothelial nitric oxide synthase (eNOS) gene is associated with coronary artery disease in non-diabetic population. 16401309 2005
Entrez Id: 7422
Gene Symbol: VEGFA
VEGFA
0.400 Biomarker disease BEFREE Vascular endothelial growth factor (VEGF) is an important active protein for the induction of angiogenesis and improvement in cardiac function after myocardial ischemia; however, the lack of a delivery system targeted to the injured myocardium reduces the local therapeutic efficacy of VEGF and increases its possible adverse effects. 19307480 2009
Entrez Id: 3949
Gene Symbol: LDLR
LDLR
0.400 GeneticVariation disease BEFREE Relationships of abdominal obesity and hyperinsulinemia to angiographically assessed coronary artery disease in men with known mutations in the LDL receptor gene. 9521335 1998
Entrez Id: 3949
Gene Symbol: LDLR
LDLR
0.400 GeneticVariation disease BEFREE Meta-analysis of low density lipoprotein receptor (LDLR) rs2228671 polymorphism and coronary heart disease. 24900971 2014
Entrez Id: 4846
Gene Symbol: NOS3
NOS3
0.400 GeneticVariation disease BEFREE Smoking-dependent and haplotype-specific effects of endothelial nitric oxide synthase gene polymorphisms on angiographically assessed coronary artery disease in Caucasian- and African-Brazilians. 16842798 2007