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SNP information rs17465637

RS17465637

Normal allele: AA

SNP of the MIA3 gene associated with increased risk of myocardial infarction with odds ratios of 1.17 (CI: 1.04-1.32) and 1.37 (CI: 1.08-1.74) for carriers.

Polymorphism rs17465637 is related to topics like this:

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Research and publications:

  17634449   Genomewide association analysis of coronary artery disease.

  18654002   Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population.

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

  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?

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

  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.

  20098575   Genetics and cardiovascular disease: Design and development of a DNA biobank.

  20159871   Association between a literature-based genetic risk score and cardiovascular events in women

  20729558   Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies.

  20835900   Genetics of diabetes complications.

  20971364   A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses.

  20981302   Genome-wide association study of coronary artery disease.

  21239051   Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.

  21264445   Extended evidence for association between the melanoma inhibitory activity 3 gene and myocardial infarction.

  21369780   Genome-wide association studies in atherosclerosis.

  21378990   Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

  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.

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

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

  21875899   Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.

  21984477   Genomic risk variants at 1p13.3, 1q41, and 3q22.3 are associated with subsequent cardiovascular outcomes in healthy controls and in established coronary artery disease.

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

  22144573   Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.

  22152955   Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies.

  22199011   Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.

  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

  22363065   Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?

  22429504   Genetic predisposition to coronary heart disease and stroke using an additive genetic risk score: a population-based study in Greece.

  22577832   Association study of MIA3 rs17465637 polymorphism with cardiovascular disease in rheumatoid arthritis patients.

  22588700   Genetics of coronary artery disease in the 21st century.

  23024462   Atherosclerosis and rheumatoid arthritis: more than a simple association.

  23236363   Meta-analyses of KIF6 Trp719Arg in coronary heart disease and statin therapeutic effect.

  23468967   Improvement in prediction of coronary heart disease risk over conventional risk factors using SNPs identified in genome-wide association studies.

  24125424   Meta-analysis identifies robust association between SNP rs17465637 in MIA3 on chromosome 1q41 and coronary artery disease.

  24932356   Genetics of coronary artery disease: an update.

  25542012   Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study.

  26252781   Potential Signals of Natural Selection in the Top Risk Loci for Coronary Artery Disease: 9p21 and 10q11.

  26847647   Experimental Biology for the Identification of Causal Pathways in Atherosclerosis.

  26892960   From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease.

  26958643   Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.

  26971241   Influence of Genetic Risk Factors on Coronary Heart Disease Occurrence in Afro-Caribbeans.

  27189168   The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease.

  27294088   Genetics of the acute coronary syndrome.

  27386434   Zinc Finger 259 Gene Polymorphism rs964184 is Associated with Serum Triglyceride Levels and Metabolic Syndrome.

  27716211   A 19-SNP coronary heart disease gene score profile in subjects with type 2 diabetes: the coronary heart disease risk in type 2 diabetes (CoRDia study) study baseline characteristics.

  28088267   A meta-analysis of three identified single nucleotide polymorphisms at 1p13.3 and 1q41 and their associations with lipid levels and coronary artery disease.

  28167353   Genetic risk analysis of coronary artery disease in Pakistani subjects using a genetic risk score of 21 variants.

  28400043   Association of the genetic markers for myocardial infarction with sudden cardiac death.

  28686695   Coronary artery disease-associated genetic variants and biomarkers of inflammation.

  28705542   Effect of Coronary Artery Disease risk SNPs on serum cytokine levels and cytokine imbalance in Premature Coronary Artery Disease.

  28856136   Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study.

  29673405   GWAS implicated risk variants in different genes contribute additively to increase the risk of coronary artery disease (CAD) in the Pakistani subjects.

  29972410   Genetic Risk Analysis of Coronary Artery Disease in a Population-based Study in Portugal, Using a Genetic Risk Score of 31 Variants.

  30571812   Additional value of a combined genetic risk score to standard cardiovascular stratification.

  31804579   The Mediterranean diet reduces the genetic risk of chromosome 9p21 for myocardial infarction in an Asian population community cohort.

  31845553   Precision Medicine and Cardiovascular Health: Insights from Mendelian Randomization Analyses.

  32237974   Statistical and Functional Studies Identify Epistasis of Cardiovascular Risk Genomic Variants From Genome-Wide Association Studies.

  33581269   Low HDL concentration in rs2048327-G carriers can predispose men to develop coronary heart disease: Tehran Cardiometabolic genetic study (TCGS).

  34137427   Genetic information improves the prediction of major adverse cardiovascular events in the GENEMACOR population.

  34276231   Epicardial Adipose Tissue: The Genetics Behind an Emerging Cardiovascular Risk Marker.

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