{{Rsnum
|rsid=7027203
|Chromosome=9
|position=93800281
|Orientation=plus
|GMAF=0.3067
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 38.1 | 48.7 | 13.3
| HCB | 62.0 | 34.3 | 3.6
| JPT | 77.9 | 22.1 | 0.0
| YRI | 40.8 | 46.9 | 12.2
| ASW | 45.6 | 43.9 | 10.5
| CHB | 62.0 | 34.3 | 3.6
| CHD | 64.2 | 33.0 | 2.8
| GIH | 57.4 | 36.6 | 5.9
| LWK | 40.9 | 46.4 | 12.7
| MEX | 41.4 | 41.4 | 17.2
| MKK | 44.9 | 40.4 | 14.7
| TSI | 51.0 | 35.3 | 13.7
| 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=C
  |Pval=6E-6
  |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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}