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SNP information rs9818870

RS9818870

Normal allele: CC

Polymorphism rs9818870 is related to topics like this:

Heart attack genetic

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Heart disease genetic

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


Research and publications:

  19198612   New susceptibility locus for coronary artery disease on chromosome 3q22.3.

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

  20440292   Early identification of cardiovascular risk using genomics and proteomics.

  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.

  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.

  21242481   Genetic risk score and risk of myocardial infarction in Hispanics.

  21297524   The 1p13.3 LDL (C)-associated locus shows large effect sizes in young populations.

  21369780   Genome-wide association studies in atherosclerosis.

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

  21733517   Fine mapping of chromosome 3q22.3 identifies two haplotype blocks in ESYT3 associated with coronary artery disease in female Han Chinese.

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

  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.

  22029572   Recent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk.

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

  22151179   Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record.

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

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

  22848412   Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts.

  22882272   Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.

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

  24991086   Novel insights into miRNA in lung and heart inflammatory diseases.

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

  26284284   Forearm vasodilator reactivity in healthy male carriers of the 3q22.3 rs9818870 polymorphism.

  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.

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

  27263109   A Single-Nucleotide Polymorphism in C12orf43 Region is Associated with the Risk of Coronary Artery Disease in a Pakistani Cohort.

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

  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.

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

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

  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.

  29264877   MRAS gene marker rs9818870 is not associated with acute coronary syndrome in the Czech population and does not predict mortality in males after acute coronary syndrome.

  32495899   Correlation between MRAS gene polymorphism and atherosclerosis.

  32858814   Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population.

  35379196   Analysis of 61 SNPs from the CAD specific genomic loci reveals unique set of SNPs as significant markers in the Southern Indian population of Hyderabad.

  22664914   miRNA-mediated regulation of gene expression is affected by disease-associated SNPs within the 3'-UTR through altered RNA structure.

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