{{Rsnum
|rsid=17261688
|Chromosome=4
|position=160107665
|Orientation=plus
|GMAF=0.06336
|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 | 79.6 | 17.7 | 2.7
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 96.5 | 3.5 | 0.0
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 86.1 | 13.9 | 0.0
| LWK | 98.2 | 1.8 | 0.0
| MEX | 82.8 | 13.8 | 3.4
| MKK | 88.5 | 11.5 | 0.0
| TSI | 73.5 | 24.5 | 2.0
| 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=G
  |Pval=3E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}