{{Rsnum
|rsid=13038095
|Chromosome=20
|position=47796832
|Orientation=plus
|GMAF=0.1042
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 84.1 | 15.0 | 0.9
| HCB | 97.8 | 2.2 | 0.0
| JPT | 91.2 | 8.8 | 0.0
| YRI | 63.3 | 34.0 | 2.7
| ASW | 71.9 | 24.6 | 3.5
| CHB | 97.8 | 2.2 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 82.2 | 16.8 | 1.0
| LWK | 68.2 | 30.0 | 1.8
| MEX | 81.0 | 19.0 | 0.0
| MKK | 75.6 | 23.1 | 1.3
| TSI | 72.5 | 27.5 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20173747
|Trait=Atrial fibrillation
|Title=Common variants in KCNN3 are associated with lone atrial fibrillation
|RiskAllele=
|Pval=2E-7
|OR=1.47
|ORtxt=[1.39-1.54]
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}