{{Rsnum
|rsid=957140
|Gene=NOX4
|Chromosome=11
|position=89468459
|Orientation=plus
|GMAF=0.4054
|Gene_s=NOX4
|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 | 16.8 | 55.8 | 27.4
| HCB | 27.7 | 51.8 | 20.4
| JPT | 35.4 | 46.9 | 17.7
| YRI | 4.1 | 34.7 | 61.2
| ASW | 3.5 | 49.1 | 47.4
| CHB | 27.7 | 51.8 | 20.4
| CHD | 27.5 | 47.7 | 24.8
| GIH | 10.9 | 42.6 | 46.5
| LWK | 9.1 | 39.1 | 51.8
| MEX | 20.7 | 51.7 | 27.6
| MKK | 14.7 | 41.7 | 43.6
| TSI | 19.6 | 51.0 | 29.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23824729
  |Trait=Homocysteine levels
  |Title=Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.
  |RiskAllele=A
  |Pval=2E-8
  |OR=.05
  |ORtxt=[0.029-0.061] unit decrease
  }}

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