{{Rsnum
|rsid=979976
|Gene=THSD7B
|Chromosome=2
|position=137011132
|Orientation=plus
|GMAF=0.3944
|Gene_s=THSD7B
|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 | 8.1 | 51.4 | 40.5
| HCB | 13.2 | 41.2 | 45.6
| JPT | 3.5 | 32.7 | 63.7
| YRI | 49.0 | 45.6 | 5.4
| ASW | 31.6 | 49.1 | 19.3
| CHB | 13.2 | 41.2 | 45.6
| CHD | 18.5 | 43.5 | 38.0
| GIH | 4.0 | 37.6 | 58.4
| LWK | 45.4 | 44.4 | 10.2
| MEX | 19.3 | 45.6 | 35.1
| MKK | 26.3 | 44.2 | 29.5
| TSI | 10.9 | 32.7 | 56.4
| 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=8E-6
  |OR=.13
  |ORtxt=[0.075-0.193] 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}}