SNP information rs2383206

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.

  18443000   Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study.

  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.

  18957718   Chromosome 9p21.3 is associated with early-onset coronary heart disease in the Irish population.

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

  19033013   Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility.

  19033589   Interaction between poor glycemic control and 9p21 locus on risk of coronary artery disease in type 2 diabetes.

  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?

  19319159   Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke.

  19329499   A genetic variant on chromosome 9p21 and incident heart failure in the ARIC study.

  19379518   Development of a fingerprinting panel using medically relevant polymorphisms.

  19559344   Genetic variants on chromosome 9p21 and ischemic stroke in Chinese.

  19578366   Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.

  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.

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

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

  20031605   9p21 is a shared susceptibility locus strongly for coronary artery disease and weakly for ischemic stroke in Chinese Han population.

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

  20565774   Population based allele frequencies of disease associated polymorphisms in the Personalized Medicine Research Project

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

  20621252   The genetics of vascular complications in diabetes mellitus.

  20691829   Joint effects of common genetic variants from multiple genes and pathways on the risk of premature coronary artery disease.

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

  20923989   Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls.

  20981302   Genome-wide association study of coronary artery disease.

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

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

  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.

  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.

  22022235   The effect of chromosome 9p21 variants on cardiovascular disease may be modified by dietary intake: evidence from a case/control and a prospective study.

  22024213   A novel gene-environment interaction involved in endometriosis

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

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

  22322877   Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established 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.

  22856518   Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21.

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

  23086272   Association between 9p21.3 genomic markers and coronary artery disease in East Asians: a meta-analysis involving 9,813 cases and 10,710 controls.

  23134948   Association between 9p21 genetic variants and mortality risk in a prospective cohort of patients with type 2 diabetes (ZODIAC-15).

  23388737   Association of single nucleotide polymorphisms on chromosome 9p21.3 with cardiovascular death in kidney transplant recipients.

  24452806   Genetic analysis of the 9p21.3 CAD risk locus in Asian Indians.

  24607648   Genetic variants at chromosome 9p21 and risk of first versus subsequent coronary heart disease events: a systematic review and meta-analysis.

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

  25105296   Polymorphism of 9p21.3 locus is associated with 5-year survival in high-risk patients with myocardial infarction.

  25361584   Subgroups at high risk for ischaemic heart disease:identification and validation in 67 000 individuals from the general population.

  25958930   Variants on Chromosome 9p21 Confer Risks of Noncardioembolic Cerebral Infarction and Carotid Plaque in the Chinese Han Population.

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

  26252781   Potential Signals of Natural Selection in the Top Risk Loci for Coronary Artery Disease: 9p21 and 10q11.

  26941057   9p21 locus rs10757278 is associated with advanced carotid atherosclerosis in a gender-specific manner.

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

  27042264   Genetics of cardiovascular and renal complications in diabetes.

  27096864   Chromosome 9p21 and ABCA1 Genetic Variants and Their Interactions on Coronary Heart Disease and Ischemic Stroke in a Chinese Han Population.

  27187494   Case-Only Survival Analysis Reveals Unique Effects of Genotype, Sex, and Coronary Disease Severity on Survivorship.

  27294088   Genetics of the acute coronary syndrome.

  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.

  27736948   The Effect of FLT1 Variant on Long-Term Cardiovascular Outcomes: Validation of a Locus Identified in a Previous Genome-Wide Association Study.

  28559532   "Desert" gene (Chr9p21) variants as novel markers for coronary artery disease.

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

  29062378   Association between rs10757274 and rs2383206 SNPs as Genetic Risk Factors in Iranian Patients with Coronary Artery Disease.

  29791233   Association of a Chromosome Locus 9p21.3 CDKN2B-AS1 Variant rs4977574 with Hypertension: The TAMRISK Study.

  30138332   Genetic variation in 9p21 is associated with fasting insulin in women but not men.

  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.

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

  30962266   Effects of ANRIL variants on the risk of ischemic stroke: 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.

  31543200   Genetic variants of chromosome 9p21.3 region associated with coronary artery disease and premature coronary artery disease in an Asian Indian population.

  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.

  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.

  34336004   Coronary Artery Disease: Association Study of 5 Loci with Angiographic Indices of Disease Severity.

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