SNP information rs6922269

Research and publications:

  17634449   Genomewide association analysis of coronary artery disease.

  18675980   Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes.

  18780302   Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.

  18852197   Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants

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

  19135198   Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease.

  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?

  19336475   Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk

  19373437   Association of three polymorphisms selected from a genome-wide association study with coronary heart disease in the Tunisian population.

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

  19777576   A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency.

  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.

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

  20981302   Genome-wide association study of 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.

  21957892   Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome.

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

  22103680   Folate network genetic variation, plasma homocysteine, and global genomic methylation content: a genetic association study.

  22216278   Large scale association analysis identifies three susceptibility loci for coronary artery disease.

  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

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

  24618918   Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients.

  25809277   Rs6922269 marker at the MTHFD1L gene predict cardiovascular mortality in males after acute coronary syndrome.

  26743840   Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma.

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

  27721851   Association of rs10757274 and rs2383206 Polymorphisms on 9p21 locus with Coronary Artery Disease in Turkish Population.

  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.

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

  32916786   Influence of SH2B3, MTHFD1L, GGCX, and ITGB3 Gene Polymorphisms on theVariability on Warfarin Dosage Requirements and Susceptibility to CVD in the Jordanian Population.

  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.