{{Rsnum
|rsid=11841001
|Gene=LMO7
|Chromosome=13
|position=75674967
|Orientation=plus
|GMAF=0.07208
|Gene_s=LMO7
|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 | 1.8 | 18.8 | 79.5
| HCB | 0.7 | 5.8 | 93.4
| JPT | 0.0 | 4.6 | 95.4
| YRI | 0.7 | 15.8 | 83.6
| ASW | 0.0 | 14.0 | 86.0
| CHB | 0.7 | 5.8 | 93.4
| CHD | 0.9 | 7.5 | 91.5
| GIH | 0.0 | 27.0 | 73.0
| LWK | 0.9 | 6.4 | 92.7
| MEX | 1.7 | 27.6 | 70.7
| MKK | 0.0 | 11.6 | 88.4
| TSI | 3.0 | 28.0 | 69.0
| 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=4E-6
  |OR=.21
  |ORtxt=[0.12-0.30] unit increase
  |OA=1
}}

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