{{Rsnum
|rsid=825411
|Gene=OPTN
|Chromosome=10
|position=13169374
|Orientation=minus
|GMAF=0.4835
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 31.0 | 47.8 | 21.2
| HCB | 13.1 | 56.2 | 30.7
| JPT | 23.0 | 49.6 | 27.4
| YRI | 28.6 | 52.4 | 19.0
| ASW | 24.6 | 42.1 | 33.3
| CHB | 13.1 | 56.2 | 30.7
| CHD | 17.4 | 50.5 | 32.1
| GIH | 27.7 | 53.5 | 18.8
| LWK | 19.1 | 55.5 | 25.5
| MEX | 22.4 | 48.3 | 29.3
| MKK | 26.3 | 50.6 | 23.1
| TSI | 25.5 | 54.9 | 19.6
| HapMapRevision=28
}}related to  [[Paget’s disease of bone]] [http://blog.23andme.com/2010/05/19/snpwatch-genetic-variants-associated-with-risk-of-pagets-disease-of-bone-identified/ 23andMe blog].

{{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}}