{{Rsnum
|rsid=6968355
|Gene=SRPK2
|Chromosome=7
|position=105117803
|Orientation=plus
|GMAF=0.09458
|Gene_s=SRPK2
|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 | 1.7 | 39.0 | 59.3
| HCB | 0.0 | 32.6 | 67.4
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 0.0 | 100.0
| ASW | 5.3 | 0.0 | 94.7
| CHB | 0.0 | 32.6 | 67.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| 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=2E-7
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}