{{Rsnum
|rsid=10824026
|Chromosome=10
|position=75421208
|Orientation=plus
|GMAF=0.3669
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=137
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 67.9 | 31.1 | 0.9
| HCB | 41.0 | 41.0 | 17.9
| JPT | 31.2 | 54.5 | 14.3
| YRI | 2.0 | 36.7 | 61.2
| ASW | 14.0 | 49.1 | 36.8
| CHB | 41.0 | 41.0 | 17.9
| CHD | 33.7 | 51.9 | 14.4
| GIH | 60.0 | 36.0 | 4.0
| LWK | 4.5 | 45.5 | 50.0
| MEX | 55.2 | 27.6 | 17.2
| MKK | 9.8 | 56.2 | 34.0
| TSI | 67.0 | 26.0 | 7.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22544366
|Trait=None
|Title=Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
|RiskAllele=A
|Pval=4E-9
|OR=1.1500
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=25196315
|Title=The rs3807989 G/A Polymorphism in CAV1 is Associated with the Risk of Atrial Fibrillation in Chinese Han Populations
}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}