{{Rsnum
|rsid=1364505
|Gene=PLXNA4
|Chromosome=7
|position=132345252
|Orientation=plus
|GMAF=0.3026
|Gene_s=PLXNA4
|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 | 7.1 | 46.0 | 46.9
| HCB | 4.4 | 28.5 | 67.2
| JPT | 2.7 | 31.0 | 66.4
| YRI | 16.3 | 51.7 | 32.0
| ASW | 12.3 | 59.6 | 28.1
| CHB | 4.4 | 28.5 | 67.2
| CHD | 2.8 | 31.2 | 66.1
| GIH | 4.0 | 27.7 | 68.3
| LWK | 21.1 | 52.3 | 26.6
| MEX | 7.0 | 24.6 | 68.4
| MKK | 21.2 | 40.4 | 38.5
| TSI | 14.7 | 44.1 | 41.2
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23509962
  |Trait=Venous thromboembolism (gene x gene interaction)
  |Title=A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis.
  |RiskAllele=A
  |Pval=2E-9
  |OR=1.80
  |ORtxt=[NR]
  |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 | FTDNA}}
{{on chip | Illumina Human 1M}}