{{Rsnum
|rsid=7044859
|Gene=CDKN2BAS
|Chromosome=9
|position=22018782
|Orientation=plus
|GMAF=0.3783
|Gene_s=CDKN2B-AS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 23.9 | 47.8 | 28.3
| HCB | 48.2 | 43.1 | 8.8
| JPT | 46.9 | 37.2 | 15.9
| YRI | 56.5 | 40.8 | 2.7
| ASW | 47.4 | 43.9 | 8.8
| CHB | 48.2 | 43.1 | 8.8
| CHD | 40.4 | 45.0 | 14.7
| GIH | 34.7 | 44.6 | 20.8
| LWK | 53.6 | 39.1 | 7.3
| MEX | 70.2 | 22.8 | 7.0
| MKK | 64.1 | 34.6 | 1.3
| TSI | 25.5 | 48.0 | 26.5
| HapMapRevision=28
}}{{PMID|17909067}} Sporadic Medullary Thyroid Carcinoma. rs7044859 alters the binding of the transcription factor HNF1

{{PMID Auto
|PMID=18675980
|Title=Novel genetic variants linked to coronary artery disease by genome-wide association are not associated with carotid artery intima-media thickness or intermediate risk phenotypes
|OA=1
}}

{{PMID|18362232|OA=1
}} Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.

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

{{PMID|19475673|OA=1
}} Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke.

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

{{PMID|20696043|OA=1
}} Replication of the association of chromosomal region 9p21.3 with generalized aggressive periodontitis (gAgP) using an independent case-control cohort.

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}