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SNP information rs2943634

RS2943634

Normal allele: AA

Polymorphism rs2943634 is related to topics like this:

Heart disease genetic

Although genetics can be a major factor in the development of certain heart diseases, individuals...


Research and publications:

  17634449   Genomewide association analysis of coronary artery disease.

  18675980   Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes.

  18780302   Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.

  18979498   The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.

  19135198   Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease.

  19164808   Large scale association analysis of novel genetic loci for coronary artery disease.

  19198609   Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.

  19207022   Genome-wide association studies of coronary artery disease and heart failure: where are we going?

  19373437   Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population.

  19750184   Genome-wide association studies for atherosclerotic vascular disease and its risk factors.

  19935834   Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart disease.

  19955471   Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study.

  19956433   Genetics of coronary artery disease: focus on genome-wide association studies.

  20017983   Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.

  20981302   Genome-wide association study of coronary artery disease.

  21133856   Genome-wide association scan allowing for epistasis in type 2 diabetes.

  21463265   Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population.

  21698238   Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population.

  21706003   Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.

  21804106   Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.

  21848424   Genetic associations with metabolic syndrome and its quantitative traits by race/ethnicity in the United States.

  21860704   Implications of discoveries from genome-wide association studies in current cardiovascular practice.

  22038522   Common genetic variants differentially influence the transition from clinically defined states of fasting glucose metabolism

  22042884   Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study.

  22207032   Significant associations of the rs2943634 (2q36.3) genetic polymorphism with adiponectin, high density lipoprotein cholesterol and ischemic stroke.

  22295058   Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Surv

  22307069   Association of type 2 diabetes susceptibility loci with one-year weight loss in the look AHEAD clinical trial

  22797928   Evidence of selection at insulin receptor substrate-1 gene loci.

  23101478   Single nucleotide polymorphisms (SNPs) involved in insulin resistance, weight regulation, lipid metabolism and inflammation in relation to metabolic syndrome: an epidemiological study.

  23659870   Common variants in and near IRS1 and subclinical cardiovascular disease in the Framingham Heart Study.

  24942486   Role of 9p21 and 2q36 variants and arterial stiffness in the prediction of coronary artery disease.

  25774817   Genetics of type 2 diabetes-pitfalls and possibilities.

  26363598   Insights into the Genetic Susceptibility to Type 2 Diabetes from Genome-Wide Association Studies of Obesity-Related Traits.

  26772723   Gene variants at FTO, 9p21, and 2q36.3 are age-independently associated with myocardial infarction in Czech men.

  27663718   Genetic variation near IRS1 is associated with adiposity and a favorable metabolic profile in U.S. Hispanics/Latinos.

  27721851   Association of rs10757274 and rs2383206 Polymorphisms on 9p21 locus with Coronary Artery Disease in Turkish Population.

  28674662   BMI prediction within a Korean population.

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