{{Rsnum
|rsid=2904524
|Gene=CNOT2
|Chromosome=12
|position=70296305
|Orientation=minus
|GMAF=0.1873
|Gene_s=CNOT2
|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 | 86.2 | 12.3 | 1.5
| HCB | 62.2 | 37.8 | 0.0
| JPT | 44.4 | 51.1 | 4.4
| YRI | 80.6 | 17.7 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 62.2 | 37.8 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 59.8 | 35.1 | 5.2
| LWK | 0.0 | 0.0 | 0.0
| MEX | 33.3 | 52.6 | 14.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22959728
  |Trait=Amyotrophic lateral sclerosis (age of onset)
  |Title=Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.
  |RiskAllele=T
  |Pval=5E-6
  |OR=NR
  |ORtxt=NR
  |OA=1
}}

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