{{Rsnum
|rsid=7644516
|Chromosome=3
|position=25880794
|Orientation=plus
|GMAF=0.06841
|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 | 82.3 | 16.8 | 0.9
| HCB | 95.5 | 4.5 | 0.0
| JPT | 93.7 | 5.4 | 0.9
| YRI | 100.0 | 0.0 | 0.0
| ASW | 93.0 | 7.0 | 0.0
| CHB | 95.5 | 4.5 | 0.0
| CHD | 98.2 | 1.8 | 0.0
| GIH | 80.2 | 18.8 | 1.0
| LWK | 97.2 | 2.8 | 0.0
| MEX | 84.5 | 15.5 | 0.0
| MKK | 93.6 | 6.4 | 0.0
| TSI | 73.3 | 25.7 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23725790
  |Trait=DNA methylation (variation)
  |Title=GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
  |RiskAllele=G
  |Pval=4E-6
  |OR=NR
  |ORtxt=NR
  }}

{{PMID Auto
|PMID=21281506
|Title=A unified framework for multi-locus association analysis of both common and rare variants.
|OA=1
}}

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