{{Rsnum
|rsid=6764363
|Gene=CHL1
|Chromosome=3
|position=270666
|Orientation=plus
|GMAF=0.2851
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CHL1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 8.0 | 48.7 | 43.4
| HCB | 0.7 | 16.1 | 83.2
| JPT | 0.0 | 31.0 | 69.0
| YRI | 19.0 | 44.9 | 36.1
| ASW | 19.3 | 43.9 | 36.8
| CHB | 0.7 | 16.1 | 83.2
| CHD | 0.9 | 18.3 | 80.7
| GIH | 11.9 | 39.6 | 48.5
| LWK | 12.7 | 49.1 | 38.2
| MEX | 3.4 | 41.4 | 55.2
| MKK | 15.4 | 51.9 | 32.7
| TSI | 16.7 | 46.1 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21658281
|Trait=None
|Title=GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
|RiskAllele=
|Pval=0.000006
|OR=1.1900
|ORtxt=[1.10-1.28]
|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}}