{{Rsnum
|rsid=10497324
|Chromosome=2
|position=167302841
|Orientation=plus
|GMAF=0.08907
|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 | 91.1 | 8.9 | 0.0
| HCB | 69.3 | 27.0 | 3.6
| JPT | 72.7 | 25.5 | 1.8
| YRI | 91.8 | 8.2 | 0.0
| ASW | 84.2 | 15.8 | 0.0
| CHB | 69.3 | 27.0 | 3.6
| CHD | 64.2 | 34.9 | 0.9
| GIH | 81.2 | 17.8 | 1.0
| LWK | 91.8 | 8.2 | 0.0
| MEX | 79.3 | 20.7 | 0.0
| MKK | 91.7 | 8.3 | 0.0
| TSI | 91.2 | 8.8 | 0.0
| 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=2E-9
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}