{{Rsnum
|rsid=3858526
|Chromosome=11
|position=5938527
|Orientation=minus
|GMAF=0.2713
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 2.7 | 38.9 | 58.4
| HCB | 3.6 | 30.7 | 65.7
| JPT | 6.2 | 47.8 | 46.0
| YRI | 12.9 | 51.0 | 36.1
| ASW | 17.5 | 45.6 | 36.8
| CHB | 3.6 | 30.7 | 65.7
| CHD | 3.7 | 31.5 | 64.8
| GIH | 5.9 | 40.6 | 53.5
| LWK | 14.7 | 44.0 | 41.3
| MEX | 15.5 | 31.0 | 53.4
| MKK | 23.1 | 50.6 | 26.3
| TSI | 6.9 | 45.1 | 48.0
| 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=C
  |Pval=3E-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}}