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SNP information rs12190287

RS12190287

Normal allele: CC

Polymorphism rs12190287 is related to topics like this:

Heart disease genetic

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

Stroke genes

Ischemic stroke has a multifactorial etiology, with genetic causes playing a significant role,...


Research and publications:

  20403199   High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.

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

  21673312   Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

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

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

  22589742   Genome-wide association of pericardial fat identifies a unique locus for ectopic fat.

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

  23874238   Disease-related growth factor and embryonic signaling pathways modulate an enhancer of TCF21 expression at the 6q23.2 coronary heart disease locus.

  24219970   Common genetic variants do not associate with CAD in familial hypercholesterolemia.

  24475106   Genetic variants associated with myocardial infarction and the risk factors in Chinese population.

  24573017   Associations between the CDKN2A/B, ADTRP and PDGFD polymorphisms and the development of coronary atherosclerosis in Japanese patients.

  24676100   Coronary heart disease-associated variation in TCF21 disrupts a miR-224 binding site and miRNA-mediated regulation.

  24932356   Genetics of coronary artery disease: an update.

  25294186   Cohen to identify the connection of the disease with rare genetic variants.

  25469254   Association of a genetic variant of the ZPR1 zinc finger gene with type 2 diabetes mellitus.

  25469260   Association of a transcription factor 21 gene polymorphism with hypertension.

  25473424   Enhancer variants: evaluating functions in common disease.

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

  26232166   Utility of a genetic risk score to predict recurrent cardiovascular events 1 year after an acute coronary syndrome: A pooled analysis of the RISCA, PRAXY, and TRIUMPH cohorts.

  26293461   Prediction of Causal Candidate Genes in Coronary Artery Disease Loci.

  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.

  26950853   Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.

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

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

  27270650   TCF21 genetic polymorphisms and breast cancer risk in Chinese women.

  27294088   Genetics of the acute coronary syndrome.

  27386823   Integrative functional genomics identifies regulatory mechanisms at coronary artery disease loci.

  27424552   Genomics era and complex disorders: Implications of GWAS with special reference to coronary artery disease, type 2 diabetes mellitus, and cancers.

  27888760   Relationship between selected DNA polymorphisms and coronary artery disease complications.

  28059143   Influence of coronary artery disease and subclinical atherosclerosis related polymorphisms on the risk of atherosclerosis in rheumatoid arthritis.

  28346832   TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population.

  28426714   A genetic risk score for CAD, psychological stress, and their interaction as predictors of CAD, fatal MI, non-fatal MI and cardiovascular death.

  28663539   Transcription Factor 21 (TCF21) rs12190287 Polymorphism is Associated with Osteosarcoma Risk and Outcomes in East Chinese Population.

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

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

  29232358   Genetic Polymorphisms of Insulin-Like Growth Factor 1 Are Associated with Osteosarcoma Risk and Prognosis.

  29435029   Nucleotide variation in ATG4A and susceptibility to cervical cancer in Southwestern Chinese women.

  29695241   Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

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

  30065929   Integrating Genes Affecting Coronary Artery Disease in Functional Networks by Multi-OMICs Approach.

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

  30774116   Functional Genetic Single-Nucleotide Polymorphisms (SNPs) in Cyclin-Dependent Kinase Inhibitor 2A/B (CDKN2A/B) Locus Are Associated with Risk and Prognosis of Osteosarcoma in Chinese Populations.

  31043074   Genetic Insights Into Smooth Muscle Cell Contributions to Coronary Artery Disease.

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

  32314747   Insulin-Like Growth Factor 1 (IGF1) Pathway Member Polymorphisms Are Associated with Risk and Prognosis of Chondrosarcoma.

  32487238   MassARRAY analysis of twelve cancer related SNPs in esophageal squamous cell carcinoma in J&K, India.

  32582717   The Role of Transcription Factor 21 in Epicardial Cell Differentiation and the Development of Coronary Heart Disease.

  32894086   MassARRAY-based single nucleotide polymorphism analysis in breast cancer of north Indian population.

  33928715   Evaluation of 17 genetic variants in association with leukemia in the north Indian population using MassARRAY Sequenom.

  34050209   Genetic evaluation of the variants using MassARRAY in non-small cell lung cancer among North Indians.

  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.

  34550115   Obesity-related genetic determinants of stroke.

  35601004   Association Between TCF21 Gene Polymorphism with the Incidence of Paroxysmal Atrial Fibrillation and the Efficacy of Radiofrequency Ablation for Patients with Paroxysmal Atrial Fibrillation.

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