{{Rsnum
|rsid=6843082
|Gene=LOC729065
|Chromosome=4
|position=110796911
|Orientation=plus
|GMAF=0.4082
|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 | 61.9 | 33.6 | 4.4
| HCB | 10.2 | 42.3 | 47.4
| JPT | 1.8 | 46.9 | 51.3
| YRI | 45.6 | 42.9 | 11.6
| ASW | 47.4 | 47.4 | 5.3
| CHB | 10.2 | 42.3 | 47.4
| CHD | 9.3 | 37.0 | 53.7
| GIH | 44.6 | 47.5 | 7.9
| LWK | 50.9 | 40.9 | 8.2
| MEX | 32.8 | 50.0 | 17.2
| MKK | 53.8 | 37.8 | 8.3
| TSI | 55.4 | 40.6 | 4.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20173747
|Trait=Atrial fibrillation
|Title=Common variants in KCNN3 are associated with lone atrial fibrillation
|RiskAllele=G
|Pval=3E-28
|OR=2.03
|ORtxt=[1.79-2.30]
|OA=1
}}

{{PharmGKB
|RSID=rs6843082
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:20173747
|Annotation=Risk or phenotype-associated allele: G . Phenotype: This variant is associated with lone atrial fibrillation. Study size: 1,335 cases; 12,844 referants. Study population/ethnicity: Cases-German AF Network, Heart and Vascular Health Study, the Cleveland Clinic and Massachusetts General Hospital. Significance metric(s): OR (for each additional minor allele) = 2.03, 95% CI = 1.79 -2.30, P = 2.5 x 10(-28) . Type of association: CO;GN
|Drugs=
|Drug Classes=
|Diseases=Atrial Fibrillation
|Curation Level=Curated
|PharmGKB Accession ID=PA165291545
}}

{{omim
|id=611494
|rsnum=6843082
}}

{{GET Evidence
|impact=pharmacogenetic
|qualified_impact=Insufficiently evaluated pharmacogenetic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6843082
|overall_frequency_n=80
|overall_frequency_d=128
|overall_frequency=0.625
|n_genomes=45
|n_genomes_annotated=0
|n_haplomes=66
|n_articles=1
|n_articles_annotated=0
|in_pharmgkb=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=23041239
  |Trait=Stroke (ischemic)
  |Title=Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.
  |RiskAllele=G
  |Pval=2E-7
  |OR=1.11
  |ORtxt=[1.06-1.15]
  |OA=1
}}

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