SNP information rs7865618

Research and publications:

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

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

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

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

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

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

  20395606   Chromosome 9p21 in ischemic stroke: population structure and meta-analysis.

  20696043   Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort.

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

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

  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.

  21858542   Sex differences in disease risk from reported genome-wide association study findings.

  22428042   Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese.

  22792221   Common variants on chromosome 9p21 are associated with normal tension glaucoma.

  24676469   Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets.

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

  25027321   Genome-wide association and admixture analysis of glaucoma from the Women's Health Initiative.

  26690118   An Updated Review on the Genetics of Primary Open Angle Glaucoma.

  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.

  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.

  27111527   Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes.

  28099408   Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202.

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

  28287809   Increased Risk of CHD in the Presence of rs7865618 (A allele): Tehran Lipid and Glucose Study.

  28347358   Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits.

  28721823   Genetic Risk Factors for Glaucoma and Exfoliation Syndrome Identified by Genome-wide Association Studies.

  29773352   The ANRIL Genetic Variants and Their Interactions with Environmental Risk Factors on Atherothrombotic Stroke in a Han Chinese Population.

  31173806   Association of CDKN2BAS gene polymorphism with periodontitis and Coronary Artery Disease from South Indian population.

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

  31632126   Genetic Analysis Of ABCA1 Gene Of Primary Glaucoma In Jordanian Arab Population.

  32509935   Dataset of allele, genotype and haplotype frequencies of five polymorphisms CDKN2B-AS1 gene in Russian patients with primary open-angle glaucoma.

  32511397   SARS-CoV2 (COVID-19) Structural/Evolution Dynamicome: Insights into functional evolution and human genomics.

  32933932   Genetic analysis of primary open-angle glaucoma-related risk alleles in a Korean population: the GLAU-GENDISK study.

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

  34387529   The haplotype of the CDKN2B-AS1 gene is associated with primary open-angle glaucoma and pseudoexfoliation glaucoma in the Caucasian population of Central Russia.

  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.

  35566612   Asian Race and Primary Open-Angle Glaucoma: Where Do We Stand?