rs13038095
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs13038095(G;G) |
| Make rs13038095(G;T) |
| Make rs13038095(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 47796832 |
| Gene | LOC107985401 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13038095 |
| dbSNP (classic) | rs13038095 |
| ClinGen | rs13038095 |
| ebi | rs13038095 |
| HLI | rs13038095 |
| Exac | rs13038095 |
| Gnomad | rs13038095 |
| Varsome | rs13038095 |
| LitVar | rs13038095 |
| Map | rs13038095 |
| PheGenI | rs13038095 |
| Biobank | rs13038095 |
| 1000 genomes | rs13038095 |
| hgdp | rs13038095 |
| ensembl | rs13038095 |
| geneview | rs13038095 |
| scholar | rs13038095 |
| rs13038095 | |
| pharmgkb | rs13038095 |
| gwascentral | rs13038095 |
| openSNP | rs13038095 |
| 23andMe | rs13038095 |
| SNPshot | rs13038095 |
| SNPdbe | rs13038095 |
| MSV3d | rs13038095 |
| GWAS Ctlg | rs13038095 |
| GMAF | 0.1042 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20173747 ]
|
| Trait | Atrial fibrillation |
| Title | Common variants in KCNN3 are associated with lone atrial fibrillation |
| Risk Allele | |
| P-val | 2E-7 |
| Odds Ratio | 1.47 [1.39-1.54] |
