{{Rsnum
|rsid=2957128
|Chromosome=18
|position=62393502
|Orientation=plus
|GMAF=0.4848
|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 | 13.3 | 54.0 | 32.7
| HCB | 60.6 | 33.6 | 5.8
| JPT | 51.3 | 39.8 | 8.8
| YRI | 17.7 | 46.9 | 35.4
| ASW | 12.3 | 47.4 | 40.4
| CHB | 60.6 | 33.6 | 5.8
| CHD | 50.5 | 42.2 | 7.3
| GIH | 20.8 | 49.5 | 29.7
| LWK | 19.3 | 52.3 | 28.4
| MEX | 20.7 | 53.4 | 25.9
| MKK | 16.7 | 49.4 | 34.0
| TSI | 12.7 | 49.0 | 38.2
| 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=A
|Pval=2E-11
|OR=1.46
|ORtxt=[1.30-1.63]
|OA=1
}}

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