{{Rsnum
|rsid=13135284
|Chromosome=4
|position=153943598
|Orientation=plus
|GMAF=0.3434
|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 | 56.6 | 34.5 | 8.8
| HCB | 47.4 | 43.8 | 8.8
| JPT | 38.1 | 51.3 | 10.6
| YRI | 39.5 | 47.6 | 12.9
| ASW | 29.8 | 45.6 | 24.6
| CHB | 47.4 | 43.8 | 8.8
| CHD | 37.6 | 47.7 | 14.7
| GIH | 36.6 | 44.6 | 18.8
| LWK | 34.5 | 50.9 | 14.5
| MEX | 24.1 | 60.3 | 15.5
| MKK | 39.1 | 42.3 | 18.6
| TSI | 52.0 | 44.1 | 3.9
| 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=C
  |Pval=5E-8
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}