{{Rsnum
|rsid=3088440
|Gene=CDKN2A
|Chromosome=9
|position=21968160
|Orientation=plus
|GMAF=0.1483
|Gene_s=CDKN2A,C9orf53
|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 | 0.0 | 22.1 | 77.9
| HCB | 2.2 | 17.0 | 80.7
| JPT | 0.0 | 14.2 | 85.8
| YRI | 4.8 | 31.3 | 63.9
| ASW | 1.8 | 26.8 | 71.4
| CHB | 2.2 | 17.0 | 80.7
| CHD | 0.0 | 20.2 | 79.8
| GIH | 2.0 | 23.2 | 74.7
| LWK | 3.7 | 34.9 | 61.5
| MEX | 14.0 | 43.9 | 42.1
| MKK | 7.3 | 32.0 | 60.7
| TSI | 1.0 | 14.9 | 84.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=19559344
|Title=Genetic variants on chromosome 9p21 and ischemic stroke in Chinese
}}

{{PMID Auto
|PMID=21061336
|Title=p14ARF genetic polymorphisms and susceptibility to second primary malignancy in patients with index squamous cell carcinoma of the head and neck
}}

{{PMID Auto
|PMID=21567202
|Title=Association analysis of p16 (CDKN2A) and RB1 polymorphisms with susceptibility to cervical cancer in Indian population
}}

{{PMID Auto
|PMID=12778444
|Title=[Polymorphism of two novel SNPs, which locate on chromosome 9p21-22, in Han Chinese of Hunan].
}}

{{PMID Auto
|PMID=17459456
|Title=A common variant of the p16(INK4a) genetic region is associated with physical function in older people.
|OA=1
}}

{{PMID Auto
|PMID=17505013
|Title=Aurora-A and p16 polymorphisms contribute to an earlier age at diagnosis of pancreatic cancer in Caucasians.
|OA=1
}}

{{PMID Auto
|PMID=18174243
|Title=Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population.
|OA=1
}}

{{PMID Auto
|PMID=18454203
|Title=Differential allelic expression in the human genome: a robust approach to identify genetic and epigenetic cis-acting mechanisms regulating gene expression.
|OA=1
}}

{{PMID Auto
|PMID=18761660
|Title=Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3.
|OA=1
}}

{{PMID Auto
|PMID=19224585
|Title=Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic.
}}

{{PMID Auto
|PMID=19258477
|Title=Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.
|OA=1
}}

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

{{PMID Auto
|PMID=20455025
|Title=Survey of familial glioma and role of germline p16INK4A/p14ARF and p53 mutation.
|OA=1
}}

{{PMID Auto
|PMID=21381012
|Title=p14ARF genetic polymorphisms and susceptibility to second primary malignancy in patients with index squamous cell carcinoma of the head and neck.
|OA=1
}}

{{PMID Auto
|PMID=23534750
|Title=Polymorphisms in TP53 (rs1042522), p16 (rs11515 and rs3088440) and NQO1 (rs1800566) Genes in Thai Cervical Cancer Patients with HPV 16 Infection
}}

{{PMID Auto
|PMID=24104554
|Title=Potentially functional variants of p14ARF are associated with HPV-positive oropharyngeal cancer patients and survival after definitive chemoradiotherapy
}}

{{PMID Auto
|PMID=23218882
|Title=Significance of MDM2 and P14 ARF polymorphisms in susceptibility to differentiated thyroid carcinoma.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}