{{Rsnum
|rsid=8028182
|Gene=SIN3A
|Chromosome=15
|position=75426328
|Orientation=plus
|GMAF=0.3136
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=SIN3A
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 67.9 | 31.2 | 0.9
| HCB | 66.4 | 29.9 | 3.6
| JPT | 56.6 | 39.8 | 3.5
| YRI | 17.7 | 46.3 | 36.1
| ASW | 24.6 | 49.1 | 26.3
| CHB | 66.4 | 29.9 | 3.6
| CHD | 65.1 | 33.0 | 1.8
| GIH | 36.6 | 48.5 | 14.9
| LWK | 5.5 | 50.5 | 44.0
| MEX | 68.4 | 29.8 | 1.8
| MKK | 21.8 | 48.7 | 29.5
| TSI | 43.1 | 42.2 | 14.7
| 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=0.000003
|OR=1.3600
|ORtxt=[1.19-1.54]
|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}}