{{Rsnum
|rsid=1151008
|Chromosome=12
|position=31944426
|Orientation=plus
|GMAF=0.3926
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 16.8 | 44.2 | 38.9
| HCB | 6.6 | 35.8 | 57.7
| JPT | 3.5 | 23.0 | 73.5
| YRI | 53.4 | 40.4 | 6.2
| ASW | 33.3 | 61.4 | 5.3
| CHB | 6.6 | 35.8 | 57.7
| CHD | 4.6 | 32.1 | 63.3
| GIH | 1.0 | 21.8 | 77.2
| LWK | 45.5 | 40.0 | 14.5
| MEX | 3.4 | 34.5 | 62.1
| MKK | 19.9 | 48.1 | 32.1
| TSI | 8.8 | 53.9 | 37.3
| 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=G
  |Pval=1E-6
  |OR=.14
  |ORtxt=[0.085-0.203] unit decrease
  |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}}