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SNP information rs11556924

RS11556924

Normal allele: CC

Polymorphism rs11556924 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:

  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.

  21737788   Network for activation of human endothelial cells by oxidized phospholipids: a critical role of heme oxygenase 1.

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

  21966275   Large-scale gene-centric analysis identifies novel variants for coronary artery disease.

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

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

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

  24932356   Genetics of coronary artery disease: an update.

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

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

  26266351   Association of Zinc Finger, C3HC-Type Containing 1 (ZC3HC1) rs11556924 Genetic Variant With Hypertension in a Finnish Population, the TAMRISK Study.

  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.

  27226629   The Coronary Artery Disease-associated Coding Variant in Zinc Finger C3HC-type Containing 1 (ZC3HC1) Affects Cell Cycle Regulation.

  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.

  28115489   Functional Validation of a Common Nonsynonymous Coding Variant in ZC3HC1 Associated With Protection From Coronary Artery Disease.

  28209224   Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.

  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.

  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.

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

  31456518   Identification of Phosphorylation Associated SNPs for Blood Pressure, Coronary Artery Disease and Stroke from Genome-wide Association Studies.

  31469255   A genome-wide association and replication study of blood pressure in Ugandan early adolescents.

  31679296   ADAMTS7 and ZC3HC1 Share Genetic Predisposition to Coronary Artery Disease and Large Artery Ischemic Stroke.

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

  31884074   Circulating Levels of Insulin-like Growth Factor 1 and Insulin-like Growth Factor Binding Protein 3 Associate With Risk of Colorectal Cancer Based on Serologic and Mendelian Randomization Analyses.

  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.

  34565088   Association of polymorphisms in endothelial dysfunction-related genes with susceptibility to essential hypertension in elderly Han population in Liaoning province, China.

  35124268   Mendelian Randomization Analysis Reveals No Causal Relationship Between Nonalcoholic Fatty Liver Disease and Severe COVID-19.

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