{{Rsnum
|rsid=11859036
|Chromosome=16
|position=80271654
|Orientation=plus
|GMAF=0.2236
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 18.6 | 51.3 | 30.1
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 4.4 | 95.6
| YRI | 2.7 | 37.7 | 59.6
| ASW | 0.0 | 42.9 | 57.1
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 1.8 | 98.2
| GIH | 3.0 | 30.7 | 66.3
| LWK | 3.6 | 30.9 | 65.5
| MEX | 1.7 | 24.1 | 74.1
| MKK | 3.2 | 35.3 | 61.5
| TSI | 14.7 | 47.1 | 38.2
| 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=7E-6
  |OR=.13
  |ORtxt=[0.071-0.185] unit increase
  |OA=1
}}

{{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 | Illumina Human 1M}}