{{Rsnum
|rsid=2926702
|Gene=NCOA2
|Chromosome=8
|position=70255759
|Orientation=minus
|GMAF=0.1887
|Gene_s=NCOA2
|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 | 78.8 | 19.5 | 1.8
| HCB | 38.2 | 43.4 | 18.4
| JPT | 26.5 | 53.1 | 20.4
| YRI | 93.2 | 6.8 | 0.0
| ASW | 96.5 | 3.5 | 0.0
| CHB | 38.2 | 43.4 | 18.4
| CHD | 33.9 | 52.3 | 13.8
| GIH | 48.5 | 46.5 | 5.0
| LWK | 88.2 | 10.9 | 0.9
| MEX | 84.5 | 15.5 | 0.0
| MKK | 87.2 | 12.2 | 0.6
| TSI | 68.6 | 26.5 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23144319
  |Trait=Non-small cell lung cancer
  |Title=Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study.
  |RiskAllele=T
  |Pval=7E-6
  |OR=NR
  |ORtxt=NR
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}