{{Rsnum
|rsid=10934011
|Chromosome=3
|position=110070723
|Orientation=plus
|GMAF=0.2787
|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 | 2.7 | 46.9 | 50.4
| HCB | 2.2 | 27.9 | 69.9
| JPT | 5.4 | 27.7 | 67.0
| YRI | 19.0 | 50.3 | 30.6
| ASW | 17.5 | 49.1 | 33.3
| CHB | 2.2 | 27.9 | 69.9
| CHD | 6.5 | 25.9 | 67.6
| GIH | 2.0 | 17.8 | 80.2
| LWK | 28.7 | 51.9 | 19.4
| MEX | 1.7 | 51.7 | 46.6
| MKK | 34.8 | 41.9 | 23.2
| TSI | 4.0 | 32.0 | 64.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23725790
  |Trait=DNA methylation (parent-of-origin)
  |Title=GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
  |RiskAllele=G
  |Pval=1E-9
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}