rs6843082
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6843082(A;A) |
| Make rs6843082(A;G) |
| Make rs6843082(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 110796911 |
| Gene | LOC729065 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6843082 |
| dbSNP (classic) | rs6843082 |
| ClinGen | rs6843082 |
| ebi | rs6843082 |
| HLI | rs6843082 |
| Exac | rs6843082 |
| Gnomad | rs6843082 |
| Varsome | rs6843082 |
| LitVar | rs6843082 |
| Map | rs6843082 |
| PheGenI | rs6843082 |
| Biobank | rs6843082 |
| 1000 genomes | rs6843082 |
| hgdp | rs6843082 |
| ensembl | rs6843082 |
| geneview | rs6843082 |
| scholar | rs6843082 |
| rs6843082 | |
| pharmgkb | rs6843082 |
| gwascentral | rs6843082 |
| openSNP | rs6843082 |
| 23andMe | rs6843082 |
| SNPshot | rs6843082 |
| SNPdbe | rs6843082 |
| MSV3d | rs6843082 |
| GWAS Ctlg | rs6843082 |
| GMAF | 0.4082 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20173747 ]
|
| Trait | Atrial fibrillation |
| Title | Common variants in KCNN3 are associated with lone atrial fibrillation |
| Risk Allele | G |
| P-val | 3E-28 |
| Odds Ratio | 2.03 [1.79-2.30] |
| GWAS snp | |
|---|---|
| PMID | [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. |
| Risk Allele | G |
| P-val | 2E-7 |
| Odds Ratio | 1.11 [1.06-1.15] |
[PMID 25711478] Association of GWAS-Supported Variants rs2200733 and rs6843082 on Chromosome 4q25 with Ischemic Stroke in the Southern Chinese Han Population
[PMID 26497660] Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF)
