{{Rsnum
|rsid=11227306
|Chromosome=11
|position=65811201
|Orientation=plus
|GMAF=0.3209
|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 | 16.8 | 49.6 | 33.6
| HCB | 15.3 | 38.7 | 46.0
| JPT | 8.0 | 44.2 | 47.8
| YRI | 8.8 | 34.0 | 57.1
| ASW | 8.8 | 45.6 | 45.6
| CHB | 15.3 | 38.7 | 46.0
| CHD | 8.3 | 45.0 | 46.8
| GIH | 0.0 | 14.9 | 85.1
| LWK | 10.9 | 40.9 | 48.2
| MEX | 8.6 | 43.1 | 48.3
| MKK | 12.2 | 50.0 | 37.8
| TSI | 15.7 | 43.1 | 41.2
| 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=A
  |Pval=2E-7
  |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}}