{{Rsnum
|rsid=484959
|Chromosome=1
|position=109823461
|Orientation=minus
|GMAF=0.4991
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 18.6 | 52.2 | 29.2
| HCB | 63.5 | 32.8 | 3.6
| JPT | 79.6 | 18.6 | 1.8
| YRI | 0.0 | 20.4 | 79.6
| ASW | 0.0 | 26.3 | 73.7
| CHB | 63.5 | 32.8 | 3.6
| CHD | 73.4 | 23.9 | 2.8
| GIH | 31.7 | 49.5 | 18.8
| LWK | 0.9 | 14.5 | 84.5
| MEX | 41.4 | 44.8 | 13.8
| MKK | 2.6 | 25.0 | 72.4
| TSI | 10.8 | 47.1 | 42.2
| 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].

{{PMID Auto GWAS
|PMID=20436471
|Trait=Paget's disease
|Title=Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone
|RiskAllele=
|Pval=5E-24
|OR=1.82
|ORtxt=[1.61-2.04]
|OA=1
}}

{{omim
|id=602080
|rsnum=484959
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}