SNP information rs1333049

Research and publications:

  17634449   Genomewide association analysis of coronary artery disease.

  18224312   Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment

  18264662   Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations.

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

  18533027   Worldwide population differentiation at disease-associated SNPs

  18599798   Coronary artery disease-associated locus on chromosome 9p21 and early markers of atherosclerosis.

  18652946   Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study.

  18654002   Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population.

  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.

  18704761   Molecular genetics of myocardial infarction.

  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

  18925945   Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study.

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

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

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

  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.

  19171343   Lack of association of chromosome 9p21.3 genotype with cardiovascular structure and function in persons with stable coronary artery disease: The Heart and Soul Study.

  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?

  19214202   Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis.

  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.

  19343170   INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis.

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

  19474294   Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

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

  19501493   A composite scoring of genotypes discriminates coronary heart disease risk beyond conventional risk factors in the Boston Puerto Rican Health Study

  19548844   Chromosome 9p21 polymorphism is associated with myocardial infarction but not with clinical outcome in Han Chinese.

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

  19664850   The 9p21.3 genotype is associated with vascular dementia and Alzheimer's disease.

  19709660   Single nucleotide polymorphism on chromosome 9p21 and endothelial progenitor cells in a general population cohort.

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

  19885677   The transcription factor GATA-2 does not associate with angiographic coronary artery disease in the Ottawa Heart Genomics and Cleveland Clinic GeneBank Studies.

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

  19924713   Use of longitudinal data in genetic studies in the genome-wide association studies era: summary of Group 14.

  19926059   No association of chromosome 9p21.3 variation with clinical and angiographic outcomes after placement of drug-eluting stents.

  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.

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

  20017983   Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.

  20031540   Association between the coronary artery disease risk locus on chromosome 9p21.3 and abdominal aortic aneurysm.

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

  20031606   The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people.

  20098575   Genetics and cardiovascular disease: Design and development of a DNA biobank.

  20159871   Association between a literature-based genetic risk score and cardiovascular events in women

  20175863   The genetics of ischaemic stroke.

  20230275   Preliminary evidence of a genetic association between chromosome 9p21.3 and human longevity.

  20231156   A variant at chromosome 9p21 is associated with recurrent myocardial infarction and cardiac death after acute coronary syndrome: the GRACE Genetics Study.

  20335276   PheWAS: demonstrating the feasibility of a phenome-wide scan to discover gene-disease associations.

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

  20395598   Association of the 9p21.3 locus with risk of first-ever myocardial infarction in Pakistanis: case-control study in South Asia and updated meta-analysis of Europeans.

  20400779   A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortality.

  20427016   Single nucleotide polymorphism rs1333049 on chromosome 9p21.3 is associated with Alzheimer's disease in Han Chinese.

  20435227   Clinical assessment incorporating a personal genome.

  20502693   Genetics and beyond--the transcriptome of human monocytes and disease susceptibility.

  20549515   Genome-wide searching of rare genetic variants in WTCCC data.

  20605023   Association of an allele on chromosome 9 and abdominal aortic aneurysm.

  20649639   Forearm vasodilator reactivity in homozygous carriers of the 9p21.3 rs1333049 G>C polymorphism.

  20670758   Gene dosage of the common variant 9p21 predicts severity of coronary artery disease.

  20858905   Association of single nucleotide polymorphisms on chromosome 9p21.3 with platelet reactivity: a potential mechanism for increased vascular disease.

  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.

  21149552   Heterogeneity of the phenotypic definition of coronary artery disease and its impact on genetic association studies.

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

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

  21270277   The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population.

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

  21362310   Polymorphism on chromosome 9p21.3 contributes to early-onset and severity of coronary artery disease in non-diabetic and type 2 diabetic patients.

  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.

  21400687   Disease and phenotype data at Ensembl.

  21424681   Peripheral arterial disease in diabetes: is there a role for genetics?

  21470412   A common polymorphism rs3781637 in MTNR1B is associated with type 2 diabetes and lipids levels in Han Chinese individuals

  21558165   Genetic association of polymorphism rs1333049 with gout.

  21606135   A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.

  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.

  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.

  21894447   Are centenarians genetically predisposed to lower disease risk?

  21971053   Genome-wide association study of coronary artery disease in the Japanese.

  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.

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

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

  22055160   Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.

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

  22199011   Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.

  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

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

  22396608   No evidence for association of Chr 9p21 variant rs1333049 with gout in New Zealand case-control sample sets.

  22400124   Genomic research to identify novel pathways in the development of abdominal aortic aneurysm.

  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.

  22429504   Genetic predisposition to coronary heart disease and stroke using an additive genetic risk score: a population-based study in Greece.

  22436605   Single polymorphism nucleotide rs1333049 on chromosome 9p21 is associated with carotid plaques but not with common carotid intima-media thickness in older adults. A combined analysis of the Three-City and the EVA studies.

  22505696   Polymorphisms of the genes encoding CD40 and growth differentiation factor 15 and in the 9p21.3 region in patients with rheumatoid arthritis and cardiovascular disease.

  22623978   A replication study of GWAS-derived lipid genes in Asian Indians: the chromosomal region 11q23.3 harbors loci contributing to triglycerides.