{{Rsnum
|rsid=7477
|Gene=CENPV
|Chromosome=17
|position=16342702
|Orientation=plus
|GMAF=0.2792
|Gene_s=CENPV,LOC102724483
|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 | 17.7 | 58.4 | 23.9
| HCB | 0.0 | 2.2 | 97.8
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.7 | 14.3 | 85.0
| ASW | 1.8 | 21.1 | 77.2
| CHB | 0.0 | 2.2 | 97.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 4.0 | 47.5 | 48.5
| LWK | 0.9 | 22.7 | 76.4
| MEX | 12.3 | 52.6 | 35.1
| MKK | 2.6 | 30.1 | 67.3
| TSI | 32.4 | 46.1 | 21.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22959728
  |Trait=Amyotrophic lateral sclerosis
  |Title=Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
  |RiskAllele=T
  |Pval=3E-7
  |OR=1.30
  |ORtxt=[1.16-1.44]
  |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 | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}