{{Rsnum
|rsid=5762311
|Chromosome=22
|position=27694209
|Orientation=plus
|GMAF=0.2897
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 15.0 | 85.0
| HCB | 27.7 | 46.7 | 25.5
| JPT | 41.6 | 42.5 | 15.9
| YRI | 13.7 | 53.4 | 32.9
| ASW | 14.0 | 35.1 | 50.9
| CHB | 27.7 | 46.7 | 25.5
| CHD | 38.5 | 51.4 | 10.1
| GIH | 8.9 | 37.6 | 53.5
| LWK | 4.6 | 30.3 | 65.1
| MEX | 8.6 | 44.8 | 46.6
| MKK | 7.7 | 41.3 | 51.0
| TSI | 2.9 | 22.5 | 74.5
| 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=0.000007
|OR=2.0300
|ORtxt=[1.49-2.75]
|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 | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}