{{Rsnum
|rsid=4141232
|Chromosome=19
|position=28544649
|Orientation=plus
|GMAF=0.1501
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LOC100420587
|Gene_s=LOC100420587,LOC101927210
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 3.6 | 28.2 | 68.2
| HCB | 3.6 | 32.1 | 64.2
| JPT | 3.5 | 38.1 | 58.4
| YRI | 0.0 | 18.4 | 81.6
| ASW | 1.8 | 14.0 | 84.2
| CHB | 3.6 | 32.1 | 64.2
| CHD | 7.3 | 33.9 | 58.7
| GIH | 4.0 | 18.8 | 77.2
| LWK | 0.9 | 10.0 | 89.1
| MEX | 1.7 | 20.7 | 77.6
| MKK | 0.0 | 15.4 | 84.6
| TSI | 7.8 | 33.3 | 58.8
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23593202
  |Trait=Femoral neck bone geometry and menarche (age at onset)
  |Title=Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche.
  |RiskAllele=
  |Pval=2E-7
  |OR=NR
  |ORtxt=NR
  |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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}