{{Rsnum
|rsid=4930103
|Chromosome=11
|position=2003314
|Orientation=plus
|GMAF=0.4536
|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 | 31.9 | 42.5 | 25.7
| HCB | 19.9 | 50.0 | 30.1
| JPT | 21.2 | 50.4 | 28.3
| YRI | 6.8 | 34.9 | 58.2
| ASW | 17.5 | 35.1 | 47.4
| CHB | 19.9 | 50.0 | 30.1
| CHD | 21.3 | 60.2 | 18.5
| GIH | 14.9 | 45.5 | 39.6
| LWK | 8.3 | 42.2 | 49.5
| MEX | 20.7 | 43.1 | 36.2
| MKK | 13.5 | 52.3 | 34.2
| TSI | 27.5 | 54.9 | 17.6
| 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=A
  |Pval=5E-16
  |OR=NR
  |ORtxt=NR
  }}

{{PMID Auto
|PMID=16839189
|Title=Human imprinted chromosomal regions are historical hot-spots of recombination.
|OA=1
}}

{{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}}