{{Rsnum
|rsid=2045084
|Gene=TSTA3
|Chromosome=8
|position=143611669
|Orientation=plus
|GMAF=0.3613
|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 | 36.3 | 42.5 | 21.2
| HCB | 5.8 | 31.4 | 62.8
| JPT | 2.7 | 27.4 | 69.9
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 22.8 | 77.2
| CHB | 5.8 | 31.4 | 62.8
| CHD | 3.7 | 32.1 | 64.2
| GIH | 9.9 | 46.5 | 43.6
| LWK | 0.0 | 3.6 | 96.4
| MEX | 22.4 | 44.8 | 32.8
| MKK | 0.0 | 25.6 | 74.4
| TSI | 37.3 | 44.1 | 18.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23585552
  |Trait=Rhegmatogenous retinal detachment
  |Title=Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.
  |RiskAllele=G
  |Pval=3E-6
  |OR=1.16
  |ORtxt=[1.09-1.24]
  }}

{{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}}