{{Rsnum
|rsid=1057510
|Gene=CHD4
|Chromosome=12
|position=6574121
|Orientation=plus
|GMAF=0.3067
|Gene_s=CHD4
|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 | 5.4 | 29.7 | 64.9
| HCB | 12.4 | 42.3 | 45.3
| JPT | 8.8 | 42.5 | 48.7
| YRI | 45.6 | 46.9 | 7.5
| ASW | 30.4 | 53.6 | 16.1
| CHB | 12.4 | 42.3 | 45.3
| CHD | 10.1 | 47.7 | 42.2
| GIH | 5.9 | 32.7 | 61.4
| LWK | 49.1 | 38.2 | 12.7
| MEX | 3.4 | 13.8 | 82.8
| MKK | 28.1 | 52.3 | 19.6
| TSI | 2.0 | 21.6 | 76.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23049088
  |Trait=Myopia (pathological)
  |Title=A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
  |RiskAllele=
  |Pval=6E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}