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SNP information rs1333040

RS1333040

Normal allele: CC

Polymorphism rs1333040 is related to topics like this:

Heart attack genetic

Genetic predisposition, also referred to as familial predisposition, is a crucial risk factor for...

Heart disease genetic

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

Stroke genes

Ischemic stroke has a multifactorial etiology, with genetic causes playing a significant role,...


Research and publications:

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

  18469204   Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians

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

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

  18997786   Susceptibility loci for intracranial aneurysm in European and Japanese populations.

  19002430   Type 2 diabetes-associated genetic variants discovered in the recent genome-wide association studies are related to gestational diabetes mellitus in the Korean population

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

  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.

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

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

  20190001   The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm.

  20364137   Genome-wide association study of intracranial aneurysm identifies three new risk loci.

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

  20395613   Confirmation of an association of single-nucleotide polymorphism rs1333040 on 9p21 with familial and sporadic intracranial aneurysms in Japanese patients.

  20595659   Differential effects of chromosome 9p21 variation on subphenotypes of intracranial aneurysm: site distribution.

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

  21146954   Genes and abdominal aortic aneurysm

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

  21315566   Type 2 diabetes and polymorphisms on chromosome 9p21: a meta-analysis.

  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.

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

  21757122   Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction.

  21896860   Association of genetic variation on chromosome 9p21 with polypoidal choroidal vasculopathy and neovascular age-related macular degeneration.

  22438818   Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure.

  22476622   Increased risk of stroke in oral contraceptive users carried replicated genetic variants: a population-based case-control study in China.

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

  22899653   Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.

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

  23606732   Association between the rs1333040 polymorphism on the chromosomal 9p21 locus and sporadic brain arteriovenous malformations.

  23733552   Genetic risk factors for intracranial aneurysms: a meta-analysis in more than 116,000 individuals.

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

  24692499   Associations between 25 lung cancer risk-related SNPs and polycyclic aromatic hydrocarbon-induced genetic damage in coke oven workers.

  24777168   Common variants on 9p21.3 are associated with brain arteriovenous malformations with accompanying arterial aneurysms.

  24860613   Genetic risk, ethnic variations and pharmacogenetic biomarkers in age-related macular degeneration and polypoidal choroidal vasculopathy.

  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.

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

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

  26186006   Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal.

  26597055   Association Study of rs1333040 and rs1004638 Polymorphisms in the 9p21 Locus with Coronary Artery Disease in Southwest of Iran.

  26732429   Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.

  26818729   Genome-wide association study of sporadic brain arteriovenous malformations.

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

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

  27317124   Long noncoding RNA dysregulation in ischemic heart failure.

  27418160   Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms.

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

  28138111   Association of CDKN2B-AS1 rs1333049 with Brain Diseases: A Case-control Study and a Meta-analysis.

  28984467   The 9p21 Rs 1333040 polymorphism is associated with coronary microvascular obstruction in ST-segment elevation myocardial infarction treated by primary angioplasty.

  29228923   CDKN2BAS gene polymorphisms and the risk of intracranial aneurysm in the Chinese 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.

  30587704   The association between the chromosome 9p21 CDKN2B-AS1 gene variants and the lipid metabolism: A pre-diagnostic biomarker for coronary artery disease.

  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.

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

  33080691   Association of ANRIL polymorphisms with coronary artery disease: A systemic meta-analysis.

  33186076   Long non-coding RNA ANRIL polymorphisms in papillary thyroid cancer and its severity.

  33285697   The association of CDKN2BAS gene polymorphisms and intracranial aneurysm: A meta-analysis.

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

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

  34511017   The rs1333040 and rs10757278 9p21 locus polymorphisms in patients with intracranial aneurysm: a meta-analysis.

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

  35470246   Associated genetic variants and potential pathogenic mechanisms of brain arteriovenous malformation.

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