{{Rsnum
|rsid=11848785
|Gene=SIPA1L1
|Chromosome=14
|position=71590638
|Orientation=plus
|GMAF=0.1556
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=SIPA1L1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 51.3 | 45.1 | 3.5
| HCB | 80.3 | 17.5 | 2.2
| JPT | 85.7 | 12.5 | 1.8
| YRI | 94.6 | 5.4 | 0.0
| ASW | 84.2 | 15.8 | 0.0
| CHB | 80.3 | 17.5 | 2.2
| CHD | 80.7 | 19.3 | 0.0
| GIH | 79.0 | 19.0 | 2.0
| LWK | 87.3 | 11.8 | 0.9
| MEX | 75.9 | 19.0 | 5.2
| MKK | 74.4 | 23.1 | 2.6
| TSI | 49.0 | 41.2 | 9.8
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21076409
|Trait=None
|Title=Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
|RiskAllele=G
|Pval=1E-10
|OR=0.5000
|ORtxt=[0.34-0.66] ms decrease
|OA=1
}}

{{PMID Auto
|PMID=24922963
|Title=163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease
}}
{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}