{{Rsnum
|rsid=1063192
|Gene=CDKN2B
|Chromosome=9
|position=22003368
|Orientation=minus
|GMAF=0.236
|Gene_s=CDKN2B,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 | 21.2 | 47.8 | 31.0
| HCB | 5.2 | 30.4 | 64.4
| JPT | 5.3 | 25.7 | 69.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 7.0 | 93.0
| CHB | 5.2 | 30.4 | 64.4
| CHD | 3.7 | 31.2 | 65.1
| GIH | 11.9 | 43.6 | 44.6
| LWK | 0.0 | 1.8 | 98.2
| MEX | 1.7 | 24.1 | 74.1
| MKK | 0.0 | 5.8 | 94.2
| TSI | 12.9 | 51.5 | 35.6
| HapMapRevision=28
}}
[[rs1063192]] is a SNP in the cyclin-dependent kinase inhibitor 2B [[CDKN2B]] gene.

A study of 432 Han Chinese patients with myocardial infarctions concluded that male subjects carrying a [[rs1063192]](C) allele were at 0.71x decreased risk (for MI).{{PMID|19272367}}

{{PMID Auto
|PMID=19559344
|Title=Genetic variants on chromosome 9p21 and ischemic stroke in Chinese
}}

{{PMID Auto GWAS
|PMID=20548946
|Trait=Vertical cup-disc ratio
|Title=A genome-wide association study of optic disc parameters
|RiskAllele=G
|Pval=4E-15
|OR=0.01
|ORtxt=[0.010-0.018] mm2 decrease
|OA=1
}}

{{PMID Auto
|PMID=21398277
|Title=Genetic variants associated with optic nerve vertical cup-to-disc ratio are risk factors for primary open angle glaucoma in a US Caucasian population
|OA=1
}}

{{PMID Auto
|PMID=22034633
|Title=Role of Noncoding RNA ANRIL in Genesis of Plexiform Neurofibromas in Neurofibromatosis Type 1
}}

{{PMID Auto
|PMID=22584021
|Title=Association between Genetic Variants Associated with Vertical Cup-to-Disc Ratio and Phenotypic Features of Primary Open-Angle Glaucoma
}}

{{PMID Auto
|PMID=22761751
|Title=CDKN2B Polymorphism Is Associated with Primary Open-Angle Glaucoma (POAG) in the Afro-Caribbean Population of Barbados, West Indies
|OA=1
}}

{{PMID Auto GWAS
|PMID=22419738
|Trait=None
|Title=A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.
|RiskAllele=T
|Pval=5E-11
|OR=1.3300
|ORtxt=None
}}

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

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

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

{{PMID Auto
|PMID=22840486
|Title=Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucoma.
}}

{{PMID Auto
|PMID=25239644
|Title=Genetic polymorphisms in the 9p21 region associated with risk of multiple cancers
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}