{{Rsnum
|rsid=9947295
|Gene=GNAL
|Chromosome=18
|position=11759433
|Orientation=plus
|GMAF=0.1942
|Gene_s=GNAL
|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 | 77.0 | 22.1 | 0.9
| HCB | 90.5 | 9.5 | 0.0
| JPT | 94.7 | 5.3 | 0.0
| YRI | 23.3 | 50.0 | 26.7
| ASW | 30.4 | 50.0 | 19.6
| CHB | 90.5 | 9.5 | 0.0
| CHD | 88.9 | 11.1 | 0.0
| GIH | 79.2 | 20.8 | 0.0
| LWK | 14.7 | 46.8 | 38.5
| MEX | 77.6 | 22.4 | 0.0
| MKK | 31.2 | 48.7 | 20.1
| TSI | 83.3 | 15.7 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23459443
  |Trait=QT interval (interaction)
  |Title=Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.
  |RiskAllele=T
  |Pval=8E-6
  |OR=NR
  |ORtxt=NR
  }}

{{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}}