{{Rsnum
|rsid=10462794
|Chromosome=5
|position=4488132
|Orientation=plus
|GMAF=0.2319
|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 | 3.6 | 34.8 | 61.6
| HCB | 0.0 | 5.8 | 94.2
| JPT | 0.0 | 3.5 | 96.5
| YRI | 11.6 | 48.3 | 40.1
| ASW | 5.3 | 40.4 | 54.4
| CHB | 0.0 | 5.8 | 94.2
| CHD | 0.0 | 5.5 | 94.5
| GIH | 14.0 | 50.0 | 36.0
| LWK | 33.0 | 36.7 | 30.3
| MEX | 6.9 | 32.8 | 60.3
| MKK | 10.3 | 47.4 | 42.3
| TSI | 8.8 | 37.3 | 53.9
| 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=C
  |Pval=5E-6
  |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}}