SNP information rs2383207

Research and publications:

  18048766   Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

  18066490   Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

  18362232   Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.

  18459066   A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease.

  18505420   Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest).

  18620593   Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome.

  18704761   Molecular genetics of myocardial infarction.

  18757290   Associations between single nucleotide polymorphisms on chromosome 9p21 and risk of coronary heart disease in Chinese Han population.

  18987759   Genetic testing for atherosclerosis risk: inevitability or pipe dream?

  19173706   The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis.

  19207022   Genome-wide association studies of coronary artery disease and heart failure: where are we going?

  19293724   The myocardial infarction associated CDKN2A/CDKN2B locus on chromosome 9p21 is associated with stroke independently of coronary events in patients with hypertension.

  19463184   Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease.

  19475673   Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.

  19592620   Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.

  19819472   Common genetic variants on chromosome 9p21 predict perioperative myocardial injury after coronary artery bypass graft surgery.

  19888323   Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants.

  19901189   A common variant at 9p21 is associated with sudden and arrhythmic cardiac death.

  19933996   Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMI.

  19956784   Association of variation in the chromosome 9p21 locus with myocardial infarction versus chronic coronary artery disease.

  20031580   Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study.

  20227257   Polymorphisms in the platelet-specific collagen receptor GP6 are associated with risk of nonfatal myocardial infarction in Caucasians

  20386740   Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.

  20601674   Bivariate genetic association of KIAA1797 with heart rate in American Indians: the Strong Heart Family Study.

  20718794   Association of polymorphisms in 9p21 region with CAD in North Indian population: replication of SNPs identified through GWAS.

  20858033   Haplotypes on 9p21 modify the risk for coronary artery disease among Indians.

  21146954   Genes and abdominal aortic aneurysm

  21152093   Sex differential genetic effect of chromosome 9p21 on subclinical atherosclerosis.

  21369780   Genome-wide association studies in atherosclerosis.

  21372283   Chromosome 9p21 haplotypes and prognosis in white and black patients with coronary artery disease.

  21375403   The relationship between polymorphisms on chromosome 9p21 and age of onset of coronary heart disease in black and white women.

  21385355   Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry.

  21415773   Chromosome 9p21 genetic variants are associated with myocardial infarction but not with ischemic stroke in a Taiwanese population.

  21698238   Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population.

  21705410   The association between variants on chromosome 9p21 and inflammatory biomarkers in ethnically diverse women with coronary heart disease: a pilot study.

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

  22122968   Additive effect of ANRIL and BRAP polymorphisms on ankle-brachial index in a Taiwanese population.

  22216169   Rationale and design of the Leipzig (LIFE) Heart Study: phenotyping and cardiovascular characteristics of patients with coronary artery disease.

  22403240   Associations between incident ischemic stroke events and stroke and cardiovascular disease-related genome-wide association studies single nucleotide polymorphisms in the Population Architecture Using Genomics and Epidemiology study.

  22844511   Common genetic variants associated with sudden cardiac death: the FinSCDgen study.

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

  22975211   Meta-analysis of genetic association of chromosome 9p21 with early-onset coronary artery disease.

  23454037   Polymorphisms on chromosome 9p21 confer a risk for acute coronary syndrome in a Chinese Han population.

  23535969   Chromosome 9p21 rs10757278 polymorphism is associated with the risk of metabolic syndrome.

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

  24875940   Evaluation of genetic association of the INK4 locus with primary open angle glaucoma in East Indian population.

  24906238   The association of 9p21-3 locus with coronary atherosclerosis: a systematic review and meta-analysis.

  25665551   Chromosome 9p21.3 Variants Are Associated with Cerebral Infarction in Chinese Population.

  26114387   Gene-Diet Interaction between SIRT6 and Soybean Intake for Different Levels of Pulse Wave Velocity.

  26944720   Polymorphisms in the long non-coding RNA CDKN2B-AS1 may contribute to higher systolic blood pressure levels in hypertensive patients.

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

  26999117   Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.

  27005424   Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease.

  27294088   Genetics of the acute coronary syndrome.

  27317124   Long noncoding RNA dysregulation in ischemic heart failure.

  27461153   Variants in 9p21 Predicts Severity of Coronary Artery Disease in a Chinese Han Population.

  27539542   Circular non-coding RNA ANRIL modulates ribosomal RNA maturation and atherosclerosis in humans.

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

  27796860   Genetic Risk Factors for Ischemic and Hemorrhagic Stroke.

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

  28716248   Interleukin-6 (IL-6) rs1800796 and cyclin dependent kinase inhibitor (CDKN2A/CDKN2B) rs2383207 are associated with ischemic stroke in indigenous West African Men.

  28813480   Paleogenetic study on the 17th century Korean mummy with atherosclerotic cardiovascular disease.

  28975602   APOL1, CDKN2A/CDKN2B, and HDAC9 polymorphisms and small vessel ischemic stroke.

  29309886   The association of polymorphic variants, rs2267788, rs1333049 and rs2383207 with coronary artery disease, its severity and presentation in North Indian population.

  29881905   LncRNA ANRIL Expression and ANRIL Gene Polymorphisms Contribute to the Risk of Ischemic Stroke in the Chinese Han Population.

  30072947   Mediating Effect of Diabetes Mellitus on the Association Between Chromosome 9p21.3 Locus and Myocardial Infarction Risk: A Case-Control Study in Shanghai, China.

  30387168   Effects of ANRIL polymorphisms on the likelihood of coronary artery disease: A meta-analysis.

  30594667   WITHDRAWN: A meta-analysis on associations of CDKN2B-AS variants with atherosclerotic cardio-cerebral vascular diseases.

  30738964   Association and interaction of genetic variants with occurrence of ischemic stroke among Brazilian patients.

  30814313   The roles of ANRIL polymorphisms in coronary artery disease: a meta-analysis.

  31055994   Genetic variants on chromosome 9p21 confer risks of cerebral infarction in the Chinese population: a meta-analysis.

  31472045   Common SNP-based haplotype analysis of the 9p21.3 gene locus as predictor coronary artery disease in Tanzanian population.

  31757599   Ischemic Stroke and Genetic Variants: In Search of Association with Severity and Recurrence in a Brazilian Population.

  32237974   Statistical and Functional Studies Identify Epistasis of Cardiovascular Risk Genomic Variants From Genome-Wide Association Studies.

  32614786   CircFOXO3 rs12196996, a polymorphism at the gene flanking intron, is associated with circFOXO3 levels and the risk of coronary artery disease.

  32696678   Associations Between Common Polymorphisms of CDKN2B-AS and Susceptibility to ASCVD.

  32840931   Association of GWAS-susceptibility loci with ischemic stroke recurrence in a Han Chinese population.

  33170161   Genetic test for the prescription of diets in support of physical activity.

  33708807   The Emerging Role of Long Non-coding RNAs and Circular RNAs in Coronary Artery Disease.

  33725991   Association between lncRNA ANRIL genetic variants with the susceptibility to ischemic stroke: From a case-control study to meta-analysis.

  34239674   Association of single-nucleotide polymorphism on chromosome 9 and ischemic stroke in Heilongjiang province in China.

  34766662   Genetic variants of PON1, GSTM1, GSTT1, and locus 9p21.3, and the risk for premature coronary artery disease in Yucatan, Mexico.

  34780941   The Association of ANRIL With Coronary Artery Disease And Aortic Aneurysms, How Far Does The Gene Desert Go?

  34817327   Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: A large-scale genetic association study.

  35028972   Significance of the lncRNAs MALAT1 and ANRIL in occurrence and development of glaucoma.

  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.