{{Rsnum
|rsid=2151280
|Gene=CDKN2BAS
|Chromosome=9
|position=22034720
|Orientation=minus
|GMAF=0.4734
|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 | 27.4 | 45.1 | 27.4
| HCB | 9.5 | 41.6 | 48.9
| JPT | 17.7 | 36.3 | 46.0
| YRI | 53.1 | 41.5 | 5.4
| ASW | 42.1 | 47.4 | 10.5
| CHB | 9.5 | 41.6 | 48.9
| CHD | 14.7 | 48.6 | 36.7
| GIH | 18.8 | 44.6 | 36.6
| LWK | 57.3 | 39.1 | 3.6
| MEX | 8.6 | 25.9 | 65.5
| MKK | 48.1 | 40.4 | 11.5
| TSI | 23.5 | 48.0 | 28.4
| HapMapRevision=28
}}
[http://blog.23andme.com/2009/07/06/snpwatch-genetic-variants-near-tumor-suppressor-genes-may-increase-risk-for-brain-and-skin-cancer/ 23andMe blog] [[rs2151280]]	G	1.19	[[Basal Cell Carcinoma]]
{{PMID Auto
|PMID=19578363
|Title=New common variants affecting susceptibility to basal cell carcinoma
|OA=1
}}

{{omim
|id=613062
|rsnum=2151280
}}

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

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}