{{Rsnum
|rsid=10494112
|Chromosome=1
|position=109809855
|Orientation=plus
|GMAF=0.1244
|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 | 67.3 | 31.0 | 1.8
| HCB | 99.3 | 0.7 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 68.0 | 28.6 | 3.4
| ASW | 70.2 | 26.3 | 3.5
| CHB | 99.3 | 0.7 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 81.0 | 17.0 | 2.0
| LWK | 79.1 | 20.0 | 0.9
| MEX | 93.1 | 6.9 | 0.0
| MKK | 74.4 | 25.0 | 0.6
| TSI | 60.4 | 34.7 | 5.0
| 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=21623375
|Trait=None
|Title=Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.
|RiskAllele=G
|Pval=7E-35
|OR=1.7200
|ORtxt=[1.57-1.87]
}}

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