{{Rsnum
|rsid=10769945
|Chromosome=11
|position=1963897
|Orientation=plus
|GMAF=0.3627
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 28.3 | 40.7 | 31.0
| HCB | 38.0 | 47.4 | 14.6
| JPT | 32.7 | 58.4 | 8.8
| YRI | 76.9 | 21.8 | 1.4
| ASW | 54.4 | 40.4 | 5.3
| CHB | 38.0 | 47.4 | 14.6
| CHD | 33.0 | 50.5 | 16.5
| GIH | 38.6 | 47.5 | 13.9
| LWK | 78.2 | 20.9 | 0.9
| MEX | 55.2 | 32.8 | 12.1
| MKK | 59.0 | 36.5 | 4.5
| TSI | 17.6 | 51.0 | 31.4
| 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=T
  |Pval=5E-7
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}