{{Rsnum
|rsid=1537370
|Gene=CDKN2B-AS1
|Chromosome=9
|position=22084311
|Orientation=plus
|GMAF=0.4073
|Gene_s=CDKN2B-AS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.1 | 48.7 | 21.2
| HCB | 10.2 | 48.9 | 40.9
| JPT | 9.7 | 38.1 | 52.2
| YRI | 3.4 | 39.5 | 57.1
| ASW | 5.3 | 57.9 | 36.8
| CHB | 10.2 | 48.9 | 40.9
| CHD | 10.1 | 39.4 | 50.5
| GIH | 18.8 | 55.4 | 25.7
| LWK | 11.8 | 37.3 | 50.9
| MEX | 24.1 | 53.4 | 22.4
| MKK | 10.9 | 44.9 | 44.2
| TSI | 14.7 | 55.9 | 29.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=23561647
|Title=Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction
}}

{{PMID Auto
|PMID=19463184
|Title=Worldwide patterns of haplotype diversity at 9p21.3, a locus associated with type 2 diabetes and coronary heart disease.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}