{{Rsnum
|rsid=11047543
|Chromosome=12
|position=24635405
|Orientation=plus
|GMAF=0.118
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 4.7 | 21.9 | 73.4
| HCB | 4.4 | 13.3 | 82.2
| JPT | 0.0 | 24.4 | 75.6
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 4.4 | 13.3 | 82.2
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20062060
|Trait=PR interval
|Title=Genome-wide association study of PR interval
|RiskAllele=A
|Pval=3E-13
|OR=2.09
|ORtxt=[1.53-2.65] ms decrease
|OA=1
}}

{{PMID Auto
|PMID=22336519
|Title=Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years
}}

{{PMID|21347284|OA=1
}} Genome-wide association studies of the PR interval in African Americans.

{{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 v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}