{{Rsnum
|rsid=17500488
|Gene=VANGL1
|Chromosome=1
|position=115669142
|Orientation=plus
|GMAF=0.1047
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=VANGL1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 15.0 | 85.0
| HCB | 2.9 | 27.7 | 69.3
| JPT | 1.8 | 34.5 | 63.7
| YRI | 0.7 | 7.5 | 91.8
| ASW | 0.0 | 21.1 | 78.9
| CHB | 2.9 | 27.7 | 69.3
| CHD | 3.7 | 27.8 | 68.5
| GIH | 0.0 | 6.9 | 93.1
| LWK | 0.0 | 2.7 | 97.3
| MEX | 0.0 | 15.5 | 84.5
| MKK | 0.6 | 17.4 | 81.9
| TSI | 1.0 | 15.7 | 83.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=21685173
|Title=Common Variants in CASQ2, GPD1L and NOS1AP Are Significantly Associated with Risk of Sudden Death in Patients with Coronary Artery Disease
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}