{{Rsnum
|rsid=11708189
|Gene=CLSTN2
|Chromosome=3
|position=140456518
|Orientation=plus
|GMAF=0.4651
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CLSTN2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 43.4 | 41.6 | 15.0
| HCB | 3.7 | 34.6 | 61.8
| JPT | 5.3 | 29.2 | 65.5
| YRI | 26.4 | 54.2 | 19.4
| ASW | 44.4 | 40.7 | 14.8
| CHB | 3.7 | 34.6 | 61.8
| CHD | 1.8 | 28.4 | 69.7
| GIH | 29.0 | 52.0 | 19.0
| LWK | 17.3 | 43.6 | 39.1
| MEX | 17.5 | 52.6 | 29.8
| MKK | 39.4 | 48.4 | 12.3
| TSI | 49.0 | 40.2 | 10.8
| 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=0.000002
|OR=1.1200
|ORtxt=[1.07-1.18]
|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}}