{{Rsnum
|rsid=3786800
|Gene=ZNF536
|Chromosome=19
|position=30499793
|Orientation=minus
|GMAF=0.1791
|Gene_s=ZNF536
|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 | 83.3 | 14.8 | 1.9
| HCB | 64.2 | 32.8 | 2.9
| JPT | 59.3 | 33.6 | 7.1
| YRI | 83.0 | 15.0 | 2.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 64.2 | 32.8 | 2.9
| CHD | 63.0 | 33.3 | 3.7
| GIH | 84.4 | 13.5 | 2.1
| LWK | 89.0 | 11.0 | 0.0
| MEX | 62.5 | 35.7 | 1.8
| MKK | 90.3 | 9.1 | 0.6
| TSI | 0.0 | 0.0 | 0.0
| 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-12
  |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}}