{{Rsnum
|rsid=4819833
|Chromosome=22
|position=19703979
|Orientation=plus
|GMAF=0.3421
|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 | 48.7 | 38.1 | 13.3
| HCB | 19.0 | 49.6 | 31.4
| JPT | 21.4 | 47.3 | 31.2
| YRI | 71.9 | 27.4 | 0.7
| ASW | 64.9 | 35.1 | 0.0
| CHB | 19.0 | 49.6 | 31.4
| CHD | 26.2 | 46.7 | 27.1
| GIH | 56.4 | 36.6 | 6.9
| LWK | 77.3 | 20.9 | 1.8
| MEX | 55.2 | 39.7 | 5.2
| MKK | 74.4 | 23.7 | 1.9
| TSI | 33.3 | 53.9 | 12.7
| 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=C
  |Pval=6E-8
  |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}}