{{Rsnum
|rsid=2070999
|Gene=NQO2
|Chromosome=6
|position=2999495
|Orientation=plus
|GMAF=0.3007
|Gene_s=NQO2
|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 | 21.2 | 42.5 | 36.3
| HCB | 7.4 | 39.0 | 53.7
| JPT | 8.0 | 41.1 | 50.9
| YRI | 0.0 | 6.8 | 93.2
| ASW | 5.3 | 14.0 | 80.7
| CHB | 7.4 | 39.0 | 53.7
| CHD | 4.6 | 42.2 | 53.2
| GIH | 14.9 | 50.5 | 34.7
| LWK | 0.0 | 9.1 | 90.9
| MEX | 14.0 | 40.4 | 45.6
| MKK | 1.3 | 21.2 | 77.6
| TSI | 13.7 | 44.1 | 42.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=24354914
|Title=NQO1 rs1800566 C&gt;T polymorphism was associated with a decreased risk of esophageal cancer in a Chinese population
}}

{{PMID Auto
|PMID=23054000
|Title=Genetic variants in metabolizing genes NQO1, NQO2, MTHFR and risk of prostate cancer: a study from North India.
}}

{{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}}