{{Rsnum
|rsid=9574199
|Gene=POU4F1-AS1
|Chromosome=13
|position=78234779
|Orientation=plus
|GMAF=0.4848
|Gene_s=POU4F1-AS1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 8.0 | 44.2 | 47.8
| HCB | 52.9 | 38.2 | 8.8
| JPT | 50.0 | 42.0 | 8.0
| YRI | 23.1 | 57.1 | 19.7
| ASW | 21.1 | 54.4 | 24.6
| CHB | 52.9 | 38.2 | 8.8
| CHD | 42.2 | 51.4 | 6.4
| GIH | 17.8 | 55.4 | 26.7
| LWK | 24.5 | 49.1 | 26.4
| MEX | 36.2 | 50.0 | 13.8
| MKK | 24.4 | 46.8 | 28.8
| TSI | 6.9 | 45.1 | 48.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21116278
|Trait=None
|Title=Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease
|RiskAllele=
|Pval=0.000007
|OR=0.0041
|ORtxt=[NR] unit increase (interaction)
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}