{{Rsnum
|rsid=724210
|Chromosome=14
|position=97057408
|Orientation=plus
|GMAF=0.1547
|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 | 51.3 | 41.6 | 7.1
| HCB | 99.3 | 0.7 | 0.0
| JPT | 99.1 | 0.9 | 0.0
| YRI | 99.3 | 0.7 | 0.0
| ASW | 87.7 | 12.3 | 0.0
| CHB | 99.3 | 0.7 | 0.0
| CHD | 98.2 | 1.8 | 0.0
| GIH | 57.4 | 38.6 | 4.0
| LWK | 93.6 | 6.4 | 0.0
| MEX | 77.6 | 20.7 | 1.7
| MKK | 84.6 | 14.7 | 0.6
| TSI | 39.2 | 48.0 | 12.7
| 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=8E-7
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}