{{Rsnum
|rsid=2891168
|Gene=CDKN2BAS
|Chromosome=9
|position=22098620
|Orientation=plus
|GMAF=0.4201
|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 | 29.2 | 49.6 | 21.2
| HCB | 24.8 | 53.3 | 21.9
| JPT | 24.8 | 48.7 | 26.5
| YRI | 75.5 | 23.1 | 1.4
| ASW | 59.6 | 35.1 | 5.3
| CHB | 24.8 | 53.3 | 21.9
| CHD | 34.9 | 38.5 | 26.6
| GIH | 29.7 | 50.5 | 19.8
| LWK | 59.6 | 34.9 | 5.5
| MEX | 25.9 | 55.2 | 19.0
| MKK | 59.0 | 37.8 | 3.2
| TSI | 16.7 | 55.9 | 27.5
| HapMapRevision=28
}}{{Report GE
|PubMed=17478681
|Source=journal
|AffyProbeset=SNP_A-2150146
|AffyOrientation=same
|AlleleA=A
|AlleleB=G
|onGW5=1
|rsid=2891168
|ancestral=A
|RiskPopulation=CEU
|RiskAllele=G
|CaseFreq=
|ControlFreq=
|OddsRatioHet=1.30
|OddsRatioHom=1.54
|OddsRatioAll=1.23
|Disease=Coronary artery disease
|DiseaseSymbol=CAD
|OA=1
}}

{{ neighbor
| rsid = 4977574
| distance = 45
}}

rs2891168 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (AG) and 1.54 times for homozygotes (GG) {{PMID|18048406}}

{{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
}}

{{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
}}

{{omim
|id=170650
|rsnum=2891168
}}

{{PMID Auto
|PMID=21949331
|Title=44 Tiling array shows low ANRIL, high CDKN2B expression associated with chromosome 9p21 coronary artery disease (CAD) risk genotype
}}

{{PMID|18987759|OA=1
}} Genetic testing for atherosclerosis risk: inevitability or pipe dream?

{{PMID|19019192}} Association of genetic variation on chromosome 9p21.3 and arterial stiffness.

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

{{PMID|19578366|OA=1
}} Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.

{{PMID|19888323|OA=1
}} Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants.

{{PMID|20403154|OA=1
}} Common genetic variants on chromosome 9p21 are associated with myocardial infarction and type 2 diabetes in an Italian population.

{{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}}