{{Rsnum
|rsid=10777845
|Chromosome=12
|position=97295990
|Orientation=plus
|GMAF=0.2672
|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 | 47.8 | 41.6 | 10.6
| HCB | 92.7 | 7.3 | 0.0
| JPT | 94.7 | 4.4 | 0.9
| YRI | 37.9 | 47.6 | 14.5
| ASW | 57.9 | 35.1 | 7.0
| CHB | 92.7 | 7.3 | 0.0
| CHD | 95.3 | 4.7 | 0.0
| GIH | 54.5 | 36.6 | 8.9
| LWK | 24.5 | 58.2 | 17.3
| MEX | 32.8 | 51.7 | 15.5
| MKK | 41.3 | 49.0 | 9.7
| TSI | 40.2 | 43.1 | 16.7
| 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=0.000005
|OR=1.1200
|ORtxt=[1.07-1.17]
|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}}