{{Rsnum
|rsid=7865618
|Gene=CDKN2BAS
|Chromosome=9
|position=22031006
|Orientation=plus
|GMAF=0.2094
|Gene_s=CDKN2B-AS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 31.0 | 48.7 | 20.4
| HCB | 83.9 | 15.3 | 0.7
| JPT | 78.8 | 18.6 | 2.7
| YRI | 100.0 | 0.0 | 0.0
| ASW | 93.0 | 7.0 | 0.0
| CHB | 83.9 | 15.3 | 0.7
| CHD | 76.1 | 22.0 | 1.8
| GIH | 44.6 | 44.6 | 10.9
| LWK | 98.2 | 1.8 | 0.0
| MEX | 74.1 | 24.1 | 1.7
| MKK | 94.2 | 5.8 | 0.0
| TSI | 37.3 | 50.0 | 12.7
| HapMapRevision=28
}}{{Report GE
|PubMed=17634449
|Source=pubmed
|AffyProbeset=SNP_A-1948244
|AffyOrientation=same
|AlleleA=A
|AlleleB=G
|onGW5=1
|rsid=7865618
|ancestral=A
|RiskPopulation=Caucasian
|RiskAllele=A
|CaseFreq=0.61
|ControlFreq=0.55
|OddsRatioHet=1.23
|OddsRatioHom=1.57
|OddsRatioAll=1.26
|Disease=Coronary artery disease
|DiseaseSymbol=CAD
|OA=1
}}

rs7865618 increases susceptibility to Coronary artery disease 1.23 times for heterozygotes (AG) and 1.57 times for homozygotes (AA) {{PMID|17634449|OA=1
}}

{{PMID Auto
|PMID=18675980
|Title=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
|OA=1
}}

{{PMID Auto
|PMID=19926059
|Title=No association of chromosome 9p21.3 variation with clinical and angiographic outcomes after placement of drug-eluting stents
}}

{{PMID Auto
|PMID=21511257
|Title=The chromosome 9p21 region and myocardial infarction in a European population
}}

{{PMID Auto GWAS
|PMID=21606135
|Trait=None
|Title=A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease.
|RiskAllele=A
|Pval=2E-27
|OR=1.1800
|ORtxt=[1.14-1.21]
|OA=1
}}

{{PMID Auto GWAS
|PMID=22428042
|Trait=None
|Title=Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese.
|RiskAllele=A
|Pval=9E-11
|OR=1.7800
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=18362232
|Title=Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.
|OA=1
}}

{{PMID Auto
|PMID=19214202
|Title=Identification of a shared genetic susceptibility locus for coronary heart disease and periodontitis.
|OA=1
}}

{{PMID Auto
|PMID=19475673
|Title=Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.
|OA=1
}}

{{PMID Auto
|PMID=20386740
|Title=Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression.
|OA=1
}}

{{PMID Auto
|PMID=20696043
|Title=Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort.
|OA=1
}}

{{PMID Auto
|PMID=24820060
|Title=Association between Polymorphisms rs1333040 and rs7865618 of Chromosome 9p21 and Sporadic Brain Arteriovenous Malformations
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Affy500k}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}