{{Rsnum
|rsid=12038826
|Gene=CAPN9
|Chromosome=1
|position=230787205
|Orientation=plus
|GMAF=0.06749
|Gene_s=CAPN9
|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 | 13.3 | 86.7
| HCB | 0.0 | 23.7 | 76.3
| JPT | 0.9 | 11.5 | 87.6
| YRI | 0.7 | 13.6 | 85.7
| ASW | 0.0 | 15.8 | 84.2
| CHB | 0.0 | 23.7 | 76.3
| CHD | 0.9 | 18.3 | 80.7
| GIH | 0.0 | 12.9 | 87.1
| LWK | 0.0 | 23.6 | 76.4
| MEX | 1.8 | 10.5 | 87.7
| MKK | 1.9 | 22.4 | 75.6
| TSI | 0.0 | 7.8 | 92.2
| 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=7E-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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}