{{Rsnum
|rsid=1333042
|Gene=CDKN2BAS
|Chromosome=9
|position=22103814
|Orientation=plus
|GMAF=0.343
|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 | 26.8 | 51.8 | 21.4
| HCB | 9.5 | 51.8 | 38.7
| JPT | 9.7 | 38.1 | 52.2
| YRI | 0.0 | 3.4 | 96.6
| ASW | 0.0 | 19.3 | 80.7
| CHB | 9.5 | 51.8 | 38.7
| CHD | 12.8 | 43.1 | 44.0
| GIH | 18.0 | 57.0 | 25.0
| LWK | 0.0 | 10.0 | 90.0
| MEX | 20.7 | 55.2 | 24.1
| MKK | 0.0 | 11.7 | 88.3
| TSI | 15.8 | 53.5 | 30.7
| HapMapRevision=28
}}

{{Report GE
|PubMed=17478681
|Source=journal
|AffyProbeset=SNP_A-4215414
|AffyOrientation=same
|AlleleA=A
|AlleleB=G
|onGW5=1
|rsid=1333042
|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
}}

rs1333042 increases susceptibility to Coronary artery disease 1.29 times for heterozygotes (AG) and 1.66 times for homozygotes (GG) {{PMID|17478679}}

rs1333042 increases susceptibility to Coronary artery disease 1.30 times for heterozygotes (AG) and 1.54 times for homozygotes (GG) {{PMID|17478681|OA=1
}}

rs1333042 increases susceptibility to Myocardial Infarction 1.36 times for heterozygotes (AG) and 1.84 times for homozygotes (GG) {{PMID|17478679}}

{{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=1333042
}}

{{PMID Auto
|PMID=18987759
|Title=Genetic testing for atherosclerosis risk: inevitability or pipe dream?
|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=19578366
|Title=Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
|OA=1
}}

{{PMID Auto GWAS
  |PMID=23364394
  |Trait=Coronary heart disease
  |Title=A genome-wide association study of a coronary artery disease risk variant.
  |RiskAllele=
  |Pval=1E-9
  |OR=1.30
  |ORtxt=[1.19-1.41]
  }}

{{PMID Auto
|PMID=22882272
|Title=Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.
|OA=1
}}

{{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}}