{{Rsnum
|rsid=3130501
|Gene=POU5F1
|Chromosome=6
|position=31168676
|Orientation=plus
|GMAF=0.2296
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=POU5F1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 6.2 | 39.8 | 54.0
| HCB | 8.8 | 43.8 | 47.4
| JPT | 21.2 | 46.9 | 31.9
| YRI | 2.0 | 21.1 | 76.9
| ASW | 0.0 | 28.1 | 71.9
| CHB | 8.8 | 43.8 | 47.4
| CHD | 10.1 | 45.9 | 44.0
| GIH | 3.0 | 40.6 | 56.4
| LWK | 1.8 | 20.0 | 78.2
| MEX | 8.6 | 31.0 | 60.3
| MKK | 2.6 | 27.6 | 69.9
| TSI | 2.9 | 32.4 | 64.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21801394
|Trait=None
|Title=Genome-Wide Association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
|RiskAllele=G
|Pval=2E-8
|OR=1.7400
|ORtxt=[1.43-2.13]
|OA=1
}}

{{PMID|17660530}} Risk alleles for multiple sclerosis identified by a genomewide study.

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}