{{Rsnum
|rsid=4683505
|Gene=CLSTN2
|Chromosome=3
|position=140528335
|Orientation=plus
|GMAF=0.135
|Gene_s=CLSTN2
|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 | 92.9 | 6.2 | 0.9
| HCB | 46.7 | 41.6 | 11.7
| JPT | 43.8 | 45.5 | 10.7
| YRI | 91.2 | 8.8 | 0.0
| ASW | 80.7 | 19.3 | 0.0
| CHB | 46.7 | 41.6 | 11.7
| CHD | 54.6 | 38.9 | 6.5
| GIH | 82.2 | 16.8 | 1.0
| LWK | 95.5 | 4.5 | 0.0
| MEX | 55.2 | 36.2 | 8.6
| MKK | 96.8 | 3.2 | 0.0
| TSI | 97.1 | 2.9 | 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=4E-7
  |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 | FTDNA}}
{{on chip | Illumina Human 1M}}