{{Rsnum
|rsid=923375
|Gene=ASPA
|Chromosome=17
|position=3489774
|Orientation=plus
|GMAF=0.2594
|Gene_s=ASPA
|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 | 4.4 | 26.5 | 69.0
| HCB | 5.9 | 42.2 | 51.9
| JPT | 5.3 | 31.9 | 62.8
| YRI | 26.0 | 47.3 | 26.7
| ASW | 26.3 | 38.6 | 35.1
| CHB | 5.9 | 42.2 | 51.9
| CHD | 7.4 | 28.7 | 63.9
| GIH | 4.0 | 34.7 | 61.4
| LWK | 19.3 | 55.0 | 25.7
| MEX | 3.5 | 17.5 | 78.9
| MKK | 22.9 | 51.0 | 26.1
| TSI | 4.9 | 35.3 | 59.8
| 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-16
  |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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}