{{Rsnum
|rsid=4142248
|Gene=ZNF285
|Chromosome=19
|position=44384114
|Orientation=plus
|GMAF=0.1093
|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 | 0.0 | 7.1 | 92.9
| HCB | 0.7 | 35.3 | 64.0
| JPT | 2.7 | 31.0 | 66.4
| YRI | 0.0 | 2.7 | 97.3
| ASW | 0.0 | 10.5 | 89.5
| CHB | 0.7 | 35.3 | 64.0
| CHD | 4.6 | 27.5 | 67.9
| GIH | 0.0 | 13.9 | 86.1
| LWK | 0.0 | 18.2 | 81.8
| MEX | 3.4 | 34.5 | 62.1
| MKK | 2.0 | 20.3 | 77.8
| TSI | 0.0 | 16.7 | 83.3
| 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=3E-15
  |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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}