{{Rsnum
|rsid=2425752
|Gene=NCOA5
|Chromosome=20
|position=46073481
|Orientation=plus
|GMAF=0.2277
|Gene_s=NCOA5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 53.1 | 43.4 | 3.5
| HCB | 55.5 | 38.0 | 6.6
| JPT | 38.9 | 45.1 | 15.9
| YRI | 99.3 | 0.7 | 0.0
| ASW | 98.2 | 1.8 | 0.0
| CHB | 55.5 | 38.0 | 6.6
| CHD | 47.7 | 41.3 | 11.0
| GIH | 59.4 | 35.6 | 5.0
| LWK | 96.4 | 3.6 | 0.0
| MEX | 56.9 | 39.7 | 3.4
| MKK | 84.0 | 14.7 | 1.3
| TSI | 48.0 | 47.1 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=21833088
  |Trait=Multiple sclerosis
  |Title=Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
  |RiskAllele=A
  |Pval=5E-10
  |OR=1.11
  |ORtxt=[1.1-1.13]
  |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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}