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SNP information rs974819

RS974819

Normal allele: CC

Polymorphism rs974819 is related to topics like this:

Heart attack genetic

Genetic predisposition, also referred to as familial predisposition, is a crucial risk factor for...

Heart disease genetic

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


Research and publications:

  21846871   A genome-wide association study in europeans and South asians identifies 5 new 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.

  22704460   A case-control study provides evidence of association for a common SNP rs974819 in PDGFD to coronary heart disease and suggests a sex-dependent effect.

  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.

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

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

  24900971   Meta-analysis of low density lipoprotein receptor (LDLR) rs2228671 polymorphism and coronary heart disease.

  24932356   Genetics of coronary artery disease: an update.

  24991929   Association of common genetic variants with lipid traits in the Indian population.

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

  26587841   Candidate Gene Analysis of Mortality in Dialysis Patients.

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

  26885234   Association study of BUD13-ZNF259 gene rs964184 polymorphism and hemorrhagic stroke risk.

  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.

  27245218   Investigation of MMP-1 genetic polymorphisms and protein expression and their effects on the risk of Kashin-Beck disease in the northwest Chinese Han population.

  27294088   Genetics of the acute coronary syndrome.

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

  28138111   Association of CDKN2B-AS1 rs1333049 with Brain Diseases: A Case-control Study and a Meta-analysis.

  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.

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

  32632093   A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine.

CGRP migraine

Migraine affects a significant portion of the adult population in most countries, with a higher...

Factor 5 blood clotting disorder

Thrombophilia, an increased tendency to form abnormal blood clots that can obstruct blood vessels,...

Memory genes

Despite being often overlooked, the brain possesses an impressive ability to restrict the creation...

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