{{Rsnum
|rsid=37060
|Gene=CNOT1
|Chromosome=16
|position=58532400
|Orientation=minus
|GMAF=0.281
|Gene_s=CNOT1
|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 | 54.5 | 41.1 | 4.5
| HCB | 40.7 | 42.2 | 17.0
| JPT | 42.5 | 43.4 | 14.2
| YRI | 74.8 | 23.1 | 2.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 40.7 | 42.2 | 17.0
| CHD | 42.2 | 45.9 | 11.9
| GIH | 43.6 | 46.5 | 9.9
| LWK | 79.1 | 20.0 | 0.9
| MEX | 24.1 | 55.2 | 20.7
| MKK | 80.0 | 16.8 | 3.2
| TSI | 54.9 | 38.2 | 6.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22726844
|Trait=None
|Title=A Common Variant in SLC8A1 Is Associated with the Duration of the Electrocardiographic QT Interval.
|RiskAllele=
|Pval=1E-7
|OR=1.5200
|ORtxt=None
|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 | Illumina Human 1M}}