{{Rsnum
|rsid=6771725
|Gene=NAALADL2
|Chromosome=3
|position=175357320
|Orientation=plus
|GMAF=0.3223
|Gene_s=NAALADL2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 44.2 | 47.8 | 8.0
| HCB | 25.0 | 53.0 | 22.0
| JPT | 23.2 | 58.9 | 17.9
| YRI | 61.4 | 37.9 | 0.7
| ASW | 70.9 | 25.5 | 3.6
| CHB | 25.0 | 53.0 | 22.0
| CHD | 23.1 | 57.7 | 19.2
| GIH | 48.5 | 39.4 | 12.1
| LWK | 62.6 | 35.5 | 1.9
| MEX | 41.1 | 44.6 | 14.3
| MKK | 72.7 | 26.0 | 1.3
| TSI | 55.9 | 38.2 | 5.9
| 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=T
  |Pval=9E-9
  |OR=2.22
  |ORtxt=[NR]
  |OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}