Cardio Genetics

SNP Prevalence and Clinical References

This page provides prevalence data for the individual SNPs among different ethnicities along with clinical references that show the risk associations. 

rs7903146
TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia
rs12255372
TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia
rs780094
The GCKR rs780094 polymorphism is associated with susceptibility of type 2 diabetes, reduced fasting plasma glucose levels, increased triglycerides levels and lower HOMA-IR in Japanese population
rs1748195
Common genetic variants contribute to primary hypertriglyceridemia without differences between familial combined hyperlipidemia and isolated hypertriglyceridemia
The role of ANGPTL3 in controlling lipoprotein metabolism
Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure patients
2016 Canadian Cardiovascular Society Guidelines for the Management of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult
Multidisciplinary strategies to treat painful mononeuropathies in the upper extremity: from lab to bedside
rs2967605
ANGPTL4 variants and their haplotypes are associated with serum lipid levels, the risk of coronary artery disease and ischemic stroke and atorvastatin cholesterol-lowering responses
ANGPTL4 in Metabolic and Cardiovascular Disease
Dietary therapy for preventing and treating coronary artery disease
Common Genetic Variants Contribute to Primary Hypertriglyceridemia Without Differences Between Familial Combined Hyperlipidemia and Isolated Hypertriglyceridemia
Association between lipoprotein lipase gene polymorphisms and cardiovascular disease risk factors in European adolescents: The Healthy Lifestyle in Europe by Nutrition in Adolescence study
rs7007797
Common Genetic Variants Contribute to Primary Hypertriglyceridemia Without Differences Between Familial Combined Hyperlipidemia and Isolated Hypertriglyceridemia
Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure patients
2016 Canadian Cardiovascular Society Guidelines for the Management of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult
Multidisciplinary strategies to treat painful mononeuropathies in the upper extremity: from lab to bedside
Genetics of type 2 diabetes and coronary artery disease and their associations with twelve cardiometabolic traits in the United Arab Emirates population
Large-scale association analysis identifies new risk loci for coronary artery disease
Coronary heart disease prevention: nutrients, foods, and dietary patterns
Polymorphisms of lipid metabolism enzyme-coding genes in patients with diabetic dyslipidemia
rs72691625
The g.-469G>A polymorphism in the GPIHBP1 gene promoter is associated with hypertriglyceridemia and has an additive effect on the risk conferred by LPL defective alleles
rs964184
Lifestyle genomics and the metabolic syndrome: A review of genetic variants that influence response to diet and exercise interventions
Zinc Finger 259 Gene Polymorphism rs964184 is Associated with Serum Triglyceride Levels and Metabolic Syndrome
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs17514846
Association of FURIN and ZPR1 polymorphisms with metabolic syndrome
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs2075291
A genetic variant c.553G>T in the apolipoprotein A5 gene is associated with an increased risk of coronary artery disease and altered triglyceride levels in a Chinese population
rs662799
Associations of polymorphisms in the apolipoprotein A1/C3/A4/A5 gene cluster with familial combined hyperlipidaemia in Hong Kong Chinese
rs3135506
Update on APOA5 Genetics: Toward a Better Understanding of Its Physiological Impact
Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene Polymorphism with Coronary Artery Disease in Moroccan Subjects: A Case-Control Study and an Updated Meta-Analysis
Influence of APOA5 (rs662799 and rs3135506) gene polymorphism in acute myocardial infarction patients and its association with basic coronary artery disease risk factors
Associations of the APOC3 rs5128 polymorphism with plasma APOC3 and lipid levels: a meta-analysis
Analysis of common and coding variants with cardiovascular disease in the diabetes heart study
Polymorphisms in the CETP, APOC3 and APOE genes in men with unstable atherosclerotic plaques in the coronary arteries
rs138326449
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
Analysis of common and coding variants with cardiovascular disease in the diabetes heart study
Influence of genetic polymorphisms on serum biomarkers of cardiac health
rs4238001
Investigation of the role of rs4238001 genetic polymorphism of SR-B1 gene on serum level of lipids in Iraqi patients with myocardial infarction treated with rosuvastatin
rs2292318
Polymorphisms of lipid metabolism enzyme-coding genes in patients with diabetic dyslipidemia
Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure patients
2016 Canadian Cardiovascular Society Guidelines for the Management of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult
rs4674344
Relationship between rs4674344 CYP27A1 gene polymorphism and coronary artery disease in a Polish population
rs10455872
Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease
rs3798221
Correlations between lipoprotein(a) gene polymorphisms and calcific aortic valve disease and coronary heart disease in Han Chinese
rs6415084
Correlations between lipoprotein(a) gene polymorphisms and calcific aortic valve disease and coronary heart disease in Han Chinese
rs7770628
Correlations between lipoprotein(a) gene polymorphisms and calcific aortic valve disease and coronary heart disease in Han Chinese
rs6752026
Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations
Associations of the APOB rs693 and rs17240441 polymorphisms with plasma APOB and lipid levels: a meta-analysis
Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population
rs515135
Large-scale association analysis identifies new risk loci for coronary artery disease
The impact of genome‐wide association studies on the pathophysiology and therapy of cardiovascular disease
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs632153
Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India
Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure patients
2016 Canadian Cardiovascular Society Guidelines for the Management of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult
Association of APOAI rs670 and APOB rs693 Gene Polymorphisms and Risk Factors for Cardiovascular Diseases in Young Brazilians and Africans.
rs1800591
Microsomal triglyceride transfer protein gene -493G/T polymorphism and its association with serum lipid levels in Bama Zhuang long-living families in China
rs599839
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
Large-scale association analysis identifies new risk loci for coronary artery disease
A common polymorphism in the LDL receptor gene has multiple effects on LDL receptor function
rs72658855
Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations
rs12071264
Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations
rs562556
Polymorphisms of rs2483205 and rs562556 in the PCSK9 gene are associated with coronary artery disease and cardiovascular risk factors
rs45613943
Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations
rs4076317
ANGPTL4 variants and their haplotypes are associated with serum lipid levels, the risk of coronary artery disease and ischemic stroke and atorvastatin cholesterol-lowering responses
Cost-effectiveness of osimertinib versus standard EGFR-TKI as first-line treatment for EGFR-mutated advanced non-small-cell lung cancer in China
rs6752026
Genetic associations between serum low LDL-cholesterol levels and variants in LDLR, APOB, PCSK9 and LDLRAP1 in African populations
Associations of the APOB rs693 and rs17240441 polymorphisms with plasma APOB and lipid levels: a meta-analysis
Variants in the APOB gene was associated with Ischemic Stroke susceptibility in Chinese Han male population
rs515135
Large-scale association analysis identifies new risk loci for coronary artery disease
The impact of genome‐wide association studies on the pathophysiology and therapy of cardiovascular disease
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs429358
Apolipoprotein E genotype, lifestyle and coronary artery disease: Gene-environment interaction analyses in the UK Biobank population
Apolipoprotein E genotype, lifestyle and coronary artery disease: Gene-environment interaction analyses in the UK Biobank population
rs17120425
Genome-Wide Association Study Identifies a Functional SIDT2 Variant Associated With HDL-C (High-Density Lipoprotein Cholesterol) Levels and Premature Coronary Artery Disease
Polymorphisms of lipid metabolism enzyme-coding genes in patients with diabetic dyslipidemia
Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure patients
2016 Canadian Cardiovascular Society Guidelines for the Management of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult
rs1532624
Relationship between CETP gene polymorphisms with coronary artery disease in Polish population
Cost-effectiveness of osimertinib versus standard EGFR-TKI as first-line treatment for EGFR-mutated advanced non-small-cell lung cancer in China
rs247616
Relationship between CETP gene polymorphisms with coronary artery disease in Polish population
Cost-effectiveness of osimertinib versus standard EGFR-TKI as first-line treatment for EGFR-mutated advanced non-small-cell lung cancer in China
rs708272
Polymorphisms of lipid metabolism enzyme-coding genes in patients with diabetic dyslipidemia
Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure patients
2016 Canadian Cardiovascular Society Guidelines for the Management of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult
APOA II genotypes frequency and their interaction with saturated fatty acids consumption on lipid profile of patients with type 2 diabetes
rs2167444
Polymorphisms rs2167444 and rs508384 in the SCD1 Gene Are Linked with High ApoB-48 Levels and Adverse Profile of Cardiometabolic Risk Factors
rs508384
Polymorphisms rs2167444 and rs508384 in the SCD1 Gene Are Linked with High ApoB-48 Levels and Adverse Profile of Cardiometabolic Risk Factors
Association between PON1 rs662 gene polymorphism and serum paraoxonase1 level in coronary artery disease patients in Northern India
rs4845625
Large-scale association analysis identifies new risk loci for coronary artery disease
IL6R haplotype rs4845625*T/rs4537545*C is a risk factor for simultaneously high CRP, LDL and ApoB levels
rs1050450
Relationship between GPX1 rs1050450 variationand the onset risk of coronary artery disease
Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure patients
2016 Canadian Cardiovascular Society Guidelines for the Management of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult
Multidisciplinary strategies to treat painful mononeuropathies in the upper extremity: from lab to bedside
rs2107545
Evaluation of the oxidative stress–related genes ALOX5, ALOX5AP, GPX1, GPX3 and MPO for contribution to the risk of type 2 diabetes mellitus in the Han Chinese population
rs1800482
The Role of Inducible NOS2 Gene Polymorphism in the Development of Essential Arterial Hypertension
rs3730017
The Role of Inducible NOS2 Gene Polymorphism in the Development of Essential Arterial Hypertension
rs1412444
Single Nucleotide Polymorphisms within LIPA (Lysosomal Acid Lipase A) Gene Are Associated with Susceptibility to Premature Coronary Artery Disease. A Replication in the Genetic of Atherosclerotic Disease (GEA) Mexican Study
rs2246833
Single Nucleotide Polymorphisms within LIPA (Lysosomal Acid Lipase A) Gene Are Associated with Susceptibility to Premature Coronary Artery Disease. A Replication in the Genetic of Atherosclerotic Disease (GEA) Mexican Study
Positive association between ALDH2 rs671 polymorphism and essential hypertension: A case-control study and meta-analysis
Dietary approaches to prevent hypertension
rs4252120
Large-scale association analysis identifies new risk loci for coronary artery disease
Association Study of Coronary Artery Disease-Associated Genome-Wide Significant SNPs with Coronary Stenosis in Pakistani Population
Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs1799963
Increased Risk for Venous Thrombosis in Carriers of the Prothrombin G→A20210 Gene Variant
rs3136516
Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study
Factor V Leiden but not the factor II 20210G>A mutation is a risk factor for premature coronary artery disease: a case-control study in Iran
rs2023938
Large-scale association analysis identifies new risk loci for coronary artery disease
Polymorphism of HDAC9 Gene Is Associated with Increased Risk of Acute Coronary Syndrome in Chinese Han Population
Common coding variant in SERPINA1 increases the risk for large artery stroke
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs10757274
Association of the rs10757274 SNP with coronary artery disease in a small group of a Pakistani population
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs1879417
Single-Nucleotide Polymorphisms in Oxidative Stress-Related Genes and the Risk of a Stroke in a Polish Population—A Preliminary Study
rs1549758
Influence of genetic polymorphisms on serum biomarkers of cardiac health
Nitric oxide synthase (NOS) single nucleotide polymorphisms are associated with coronary heart disease and hypertension in the INTERGENE study
rs2070744
Endothelial nitric oxide synthase gene single nucleotide polymorphisms and the risk of hypertension: A meta-analysis involving 63,258 subjects
rs3918226
Target Sequencing, Cell Experiments, and a Population Study Establish Endothelial Nitric Oxide Synthase (eNOS) Gene as Hypertension Susceptibility Gene
Endothelial Nitric Oxide Synthase Polymorphism rs3918226 Associated With Hypertension Does Not Affect Plasma Nitrite Levels in Healthy Subjects
rs1799983
Association between eNOS rs1799983 polymorphism and hypertension: a meta-analysis involving 14,185 cases and 13,407 controls
rs2271037
Association of rs2271037 and rs3749585 polymorphisms in CORIN with susceptibility to hypertension in a Chinese Han population: A case-control study
rs3749585
Association of rs2271037 and rs3749585 polymorphisms in CORIN with susceptibility to hypertension in a Chinese Han population: A case-control study
rs75770792
Corin Gene Minor Allele Defined by 2 Missense Mutations Is Common in Blacks and Associated With High Blood Pressure and Hypertension
rs111253292
Corin Gene Minor Allele Defined by 2 Missense Mutations Is Common in Blacks and Associated With High Blood Pressure and Hypertension
rs9332982
A common polymorphism of CYP4A11 is associated with blood pressure in a Chinese population
rs1799998
Reevaluation of the association of seven candidate genes with blood pressure and hypertension: a replication study and meta-analysis with a larger sample size
Association between Aldosterone Synthase (CYP11B2) Gene Polymorphism and Hypertension in Pashtun Ethnic Population of Khyber Pakhtunkwha, Pakistan
rs1126742
A haplotype of the CYP4A11 gene associated with essential hypertension in Japanese men
GENETIC VARIATION IN CYP4A11 AND BLOOD PRESSURE RESPONSE TO MINERALOCORTICOID RECEPTOR ANTAGONISM OR ENAC INHIBITION: AN EXPLORATORY PILOT STUDY IN AFRICAN AMERICANS
rs2108622
CYP4F2 genetic polymorphisms are associated with coronary heart disease in a Chinese population
Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure patients
2016 Canadian Cardiovascular Society Guidelines for the Management of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult
Multidisciplinary strategies to treat painful mononeuropathies in the upper extremity: from lab to bedside
α-Adducin gene G614T polymorphisms in essential hypertension patients with high low density lipoprotein (LDL) levels
α-adducin Gly460Trp polymorphism and essential hypertension risk in Chinese: a meta-analysis
Association of alpha-ADD1 Gene and Hypertension Risk: A Meta-Analysis
Dietary approaches to prevent hypertension
Polymorphisms of the Endothelin-1 Gene Associate with Hypertension in Patients with Rheumatoid Arthritis
rs12526453
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction
rs169713
A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1
Derin Ven Trombozundan Korunmada AkdenizDiyetinin Rolü
rs10116277
The Relationship Between Polymorphisms on Chromosome 9p21 and Age of Onset of Coronary Heart Disease in Black and White Women
rs4977574
Large Scale Association Analysis Identifies Three Susceptibility Loci for Coronary Artery Disease
The 9p21 Myocardial Infarction Risk Allele Increases Risk of Peripheral Artery Disease in Older People
rs1333049
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
The Coronary Artery Disease–Associated 9p21 Variant and Later Life 20-Year Survival to Cohort Extinction
rs10757278
A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction
rs2383207
Associations Between Single Nucleotide Polymorphisms on Chromosome 9p21 and Risk of Coronary Heart Disease in Chinese Han Population
rs2383206
Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population
rs1801133
Genetic polymorphism of MTHFR C677T and premature coronary artery disease susceptibility: A meta-analysis
rs1801131
Association of methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms with coronary artery disease (CAD) in a North Indian population
The association of methylene tetrahydrofolate reductase (MTHFR) A1298C gene polymorphism, homocysteine, vitamin B12, and folate with coronary artery disease (CAD) in the north of Iran
Identification of an association between coronary heart disease and ITGB2 methylation in peripheral blood by a case-control study
Potential Impact of COMT-rs4680 G > A Gene Polymorphism in Coronary Artery Disease
Mediterranean diet improves dyslipidemia and biomarkers in chronic renal failure patients
2016 Canadian Cardiovascular Society Guidelines for the Management of Dyslipidemia for the Prevention of Cardiovascular Disease in the Adult
Multidisciplinary strategies to treat painful mononeuropathies in the upper extremity: from lab to bedside
rs1761667
CD36 gene polymorphism rs1761667 (G > A) is associated with hypertension and coronary artery disease in an Iranian population
rs1042714
β2-Adrenergic Receptor Gene Polymorphisms Are Associated with Cardiovascular Events But not All-Cause Mortality in Coronary Artery Disease Patients: A Meta-Analysis of Prospective Studies
rs1122608
Correlation of rs1122608 SNP with acute myocardial infarction susceptibility and clinical characteristics in a Chinese Han population: A case-control study
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs10947789
Large-scale association analysis identifies new risk loci for coronary artery disease
The SH2B3 and KCNK5 loci may be implicated in regulation of platelet count, volume, and maturity
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs9982601
Large-scale association analysis identifies new risk loci for coronary artery disease
The rs9982601 polymorphism of the region between the SLC5A3/MRPS6 and KCNE2 genes associated with a prevalence of myocardial infarction and subsequent long-term mortality
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs11556924
Functional Validation of a Common Nonsynonymous Coding Variant in ZC3HC1 Associated With Protection From Coronary Artery Disease
Association of Zinc Finger, C3HC-Type Containing 1 (ZC3HC1) rs11556924 Genetic Variant With Hypertension in a Finnish Population, the TAMRISK Study
The Coronary Artery Disease-associated Coding Variant in Zinc Finger C3HC-type Containing 1 (ZC3HC1) Affects Cell Cycle Regulation*
Coronary heart disease prevention: nutrients, foods, and dietary patterns
rs2010963
Vascular endothelial growth factor A polymorphisms are associated with increased risk of coronary heart disease: a meta-analysis
Dietary approaches to prevent hypertension
Association of AGTR1 (rs5186), VDR (rs2228570) genespolymorphism with blood pressure elevation inpatients with essential arterial hypertension
Angiotensin II type 1 receptor polymorphisms and susceptibility to hypertension: A HuGE review
RAS gene polymorphisms, classical risk factors and the advent of coronary artery disease in the Portuguese population
A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor
Dietary approaches to prevent hypertension
rs4646994
Angiotensin converting enzyme insertion/deletion (I/D) (rs4646994) and Vegf polymorphism (+405G/C; rs2010963) in type II diabetic patients: Association with the risk of coronary artery disease
Reevaluation of the association of seven candidate genes with blood pressure and hypertension: a replication study and meta-analysis with a larger sample size
Gender-Related Association of AGT Gene Variants (M235T and T174M) with Essential Hypertension—A Case-Control Study
Dietary approaches to prevent hypertension
POLYMORPHIC VARIANTS OF AGT (RS4762) AND GNB3 (RS5443) GENES AS RISK FACTORS FOR SEVERE ARTERIAL HYPERTENSION
Dietary approaches to prevent hypertension
Dietary approaches to prevent hypertension
rs2200733
Variants conferring risk of atrial fibrillation on chromosome 4q25
Variants conferring risk of atrial fibrillation on chromosome 4q25
rs10033464
Variants conferring risk of atrial fibrillation on chromosome 4q25
The 4q25 variant rs13143308T links risk of atrial fibrillation to defective calcium homoeostasis
rs776746
ОСОБЕННОСТИ РАСПРЕДЕЛЕНИЯ ПОЛИМОРФИЗМОВ ГЕНОВ МЕТАБОЛИЗМА И ТРАНСПОРТА СТАТИНОВ В ПЕЧЕНИ У БОЛЬНЫХ ИБС ЭТНИЧЕСКИХ УЗБЕКОВ С НЕПЕРЕНОСИМОСТЬЮ СИМВАСТАТИНА
rs2231142
ОСОБЕННОСТИ РАСПРЕДЕЛЕНИЯ ПОЛИМОРФИЗМОВ ГЕНОВ МЕТАБОЛИЗМА И ТРАНСПОРТА СТАТИНОВ В ПЕЧЕНИ У БОЛЬНЫХ ИБС ЭТНИЧЕСКИХ УЗБЕКОВ С НЕПЕРЕНОСИМОСТЬЮ СИМВАСТАТИНА
rs4149056
The influence of genetic polymorphisms in drug metabolism enzymes and transporters on the pharmacokinetics of different fluvastatin formulations
rs1057910
Lipid-lowering effect of fluvastatin in relation to cytochrome P450 2C9 variant alleles frequently distributed in the Czech population
Cytochrome P450 2C9-CYP2C9
rs20455
Association of the Trp719Arg polymorphism in kinesin-like protein 6 with myocardial infarction and coronary heart disease in 2 prospective trials: the CARE and WOSCOPS trials
c388A > G (AKA rs2306283)
Disposition of ezetimibe is influenced by polymorphisms of the hepatic uptake carrier OATP1B1
rs7757336
Genetic polymorphism of organic cation transporter 2 (OCT2) and its effects on the pharmacokinetics and pharmacodynamics of Metformin: a narrative review
rs201919874
Genetic polymorphism of organic cation transporter 2 (OCT2) and its effects on the pharmacokinetics and pharmacodynamics of Metformin: a narrative review
rs2071746
Genetic Polymorphisms of HO-1 and COX-1 Are Associated With Aspirin Resistance Defined by Light Transmittance Aggregation in Chinese Han Patients
rs1330344
Genetic Polymorphisms of HO-1 and COX-1 Are Associated With Aspirin Resistance Defined by Light Transmittance Aggregation in Chinese Han Patients
rs4918758
Polymorphisms of Aspirin-Metabolizing Enzymes CYP2C9, NAT2 and UGT1A6 in Aspirin-Intolerant Urticaria
rs3798220
Aspirin for Primary Prevention of Cardiovascular Events in Relation to Lipoprotein(a) Genotypes
Coronary artery disease and the risk-associated LPA variants, rs3798220 and rs10455872, in patients with suspected familial hypercholesterolaemia
rs4244285
CYP2C19*2 gene variant (G681A, rs4244285) as a prognostic marker for the clinical course of multiple myeloma
Cyp2C19*2 Polymorphism Related to Clopidogrel Resistance in Patients With Coronary Heart Disease, Especially in the Asian Population: A Systematic Review and Meta-Analysis
Genetic polymorphism of clopidogrel metabolism related gene CYP2C19 gene in Chinese from Foshan area of Guangdong Province
Genetic polymorphism of angiotensin converting enzyme and angiotensin II type 1 receptors and their impact on the outcome of acute coronary syndrome
Genetic polymorphism of angiotensin converting enzyme and angiotensin II type 1 receptors and their impact on the outcome of acute coronary syndrome
rs1799722
Cross-sectional study of the association of 5 single nucleotide polymorphisms with enalapril treatment response among South African adults with hypertension
rs738409
The I148M PNPLA3 variant mitigates niacin beneficial effects: How the genetic screening in non-alcoholic fatty liver disease patients gains value
rs1944438
Dietary Niacin Intake Predicts the Decrease of Liver Fat Content During a Lifestyle Intervention
rs1800566
Association between genetic variants in the Coenzyme Q10 metabolism and Coenzyme Q10 status in humans
rs762551
Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension
Association of AGTR1 A1166C and CYP2C9∗3 Gene Polymorphisms with the Antihypertensive Effect of Valsartan