{{Rsnum
|rsid=1004689
|Chromosome=22
|position=48256185
|Orientation=plus
|GMAF=0.4945
|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 | 15.0 | 33.6 | 51.3
| HCB | 26.3 | 51.8 | 21.9
| JPT | 42.5 | 40.7 | 16.8
| YRI | 70.7 | 27.2 | 2.0
| ASW | 56.1 | 36.8 | 7.0
| CHB | 26.3 | 51.8 | 21.9
| CHD | 30.3 | 50.5 | 19.3
| GIH | 21.8 | 38.6 | 39.6
| LWK | 76.4 | 22.7 | 0.9
| MEX | 12.1 | 50.0 | 37.9
| MKK | 69.2 | 30.1 | 0.6
| TSI | 11.8 | 49.0 | 39.2
| 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=G
  |Pval=2E-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}}