{{Rsnum
|rsid=2281727
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SMG6
|position=2214651
|Gene_s=SMG6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 9.7 | 48.7 | 41.6
| HCB | 4.4 | 45.3 | 50.4
| JPT | 4.4 | 38.1 | 57.5
| YRI | 25.9 | 45.6 | 28.6
| ASW | 14.0 | 42.1 | 43.9
| CHB | 4.4 | 45.3 | 50.4
| CHD | 11.9 | 39.4 | 48.6
| GIH | 15.8 | 48.5 | 35.6
| LWK | 30.9 | 48.2 | 20.9
| MEX | 5.2 | 41.4 | 53.4
| MKK | 41.3 | 45.2 | 13.5
| TSI | 16.7 | 52.9 | 30.4
| HapMapRevision=28
}}

{{PMID Auto
|PMID=3679547
|Title=Large-scale association analysis identifies new risk loci for coronary artery disease
}}

{{PMID Auto GWAS
  |PMID=24262325
  |Trait=Coronary artery disease
  |Title=Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
  |RiskAllele=G
  |Pval=1E-7
  |OR=1.07
  |ORtxt=[1.04-1.10]
  }}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}