{{Rsnum
|rsid=1164064
|Chromosome=3
|position=109743553
|Orientation=plus
|GMAF=0.3751
|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 | 18.6 | 47.8 | 33.6
| HCB | 9.5 | 32.1 | 58.4
| JPT | 15.0 | 35.4 | 49.6
| YRI | 12.2 | 47.6 | 40.1
| ASW | 24.6 | 35.1 | 40.4
| CHB | 9.5 | 32.1 | 58.4
| CHD | 9.2 | 41.3 | 49.5
| GIH | 5.9 | 52.5 | 41.6
| LWK | 14.5 | 43.6 | 41.8
| MEX | 10.3 | 46.6 | 43.1
| MKK | 12.2 | 48.1 | 39.7
| TSI | 20.6 | 52.9 | 26.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23761726
  |Trait=Corneal astigmatism
  |Title=Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: Results of a genome-wide association study.
  |RiskAllele=A
  |Pval=2E-6
  |OR=.13
  |ORtxt=[0.079-0.189] unit increase
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}