{{Rsnum
|rsid=10012307
|Chromosome=4
|position=136605429
|Orientation=plus
|GMAF=0.2672
|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 | 0.0 | 12.4 | 87.6
| HCB | 12.7 | 41.0 | 46.3
| JPT | 9.9 | 59.5 | 30.6
| YRI | 29.5 | 51.4 | 19.2
| ASW | 33.3 | 52.6 | 14.0
| CHB | 12.7 | 41.0 | 46.3
| CHD | 8.3 | 56.9 | 34.9
| GIH | 3.0 | 24.8 | 72.3
| LWK | 34.5 | 48.2 | 17.3
| MEX | 0.0 | 17.5 | 82.5
| MKK | 32.3 | 44.5 | 23.2
| TSI | 0.0 | 7.9 | 92.1
| 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=T
  |Pval=2E-8
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}