{{Rsnum
|rsid=2555155
|Gene=DNHD1
|Chromosome=11
|position=6501574
|Orientation=minus
|GMAF=0.4963
|Gene_s=DNHD1
|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 | 25.7 | 41.6 | 32.7
| HCB | 63.5 | 32.8 | 3.6
| JPT | 55.9 | 38.7 | 5.4
| YRI | 4.8 | 34.2 | 61.0
| ASW | 14.0 | 40.4 | 45.6
| CHB | 63.5 | 32.8 | 3.6
| CHD | 67.9 | 29.4 | 2.8
| GIH | 27.7 | 43.6 | 28.7
| LWK | 5.5 | 43.6 | 50.9
| MEX | 18.2 | 54.5 | 27.3
| MKK | 14.1 | 52.6 | 33.3
| TSI | 9.8 | 53.9 | 36.3
| 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=G
  |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 | FTDNA}}
{{on chip | Illumina Human 1M}}