{{Rsnum
|rsid=4304977
|Chromosome=15
|position=92263061
|Orientation=plus
|GMAF=0.4513
|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 | 26.5 | 44.2 | 29.2
| HCB | 27.7 | 48.2 | 24.1
| JPT | 15.0 | 53.1 | 31.9
| YRI | 52.4 | 40.8 | 6.8
| ASW | 57.9 | 31.6 | 10.5
| CHB | 27.7 | 48.2 | 24.1
| CHD | 23.9 | 43.1 | 33.0
| GIH | 32.7 | 42.6 | 24.8
| LWK | 59.1 | 32.7 | 8.2
| MEX | 27.6 | 56.9 | 15.5
| MKK | 51.9 | 35.9 | 12.2
| TSI | 30.4 | 43.1 | 26.5
| 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=5E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}