{{Rsnum
|rsid=9596905
|Chromosome=13
|position=54059238
|Orientation=plus
|GMAF=0.1286
|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 | 0.0 | 9.2 | 90.8
| HCB | 2.2 | 13.3 | 84.4
| JPT | 0.0 | 15.6 | 84.4
| YRI | 13.7 | 45.3 | 41.0
| ASW | 16.4 | 47.3 | 36.4
| CHB | 2.2 | 13.3 | 84.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 1.0 | 19.0 | 80.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 8.6 | 48.7 | 42.8
| TSI | 1.0 | 21.4 | 77.6
| 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=A
  |Pval=2E-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}}