{{Rsnum
|rsid=496892
|Gene=CDKN2BAS
|Chromosome=9
|position=22024352
|Orientation=plus
|GMAF=0.3508
|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 | 20.0 | 49.2 | 30.8
| HCB | 6.7 | 37.8 | 55.6
| JPT | 13.3 | 44.4 | 42.2
| YRI | 3.2 | 39.7 | 57.1
| ASW | 0.0 | 0.0 | 0.0
| CHB | 6.7 | 37.8 | 55.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{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=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|18362232|OA=1
}} Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.

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

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

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

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

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}