rs11720524
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11720524(C;C) |
| Make rs11720524(C;G) |
| Make rs11720524(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 38633921 |
| Gene | SCN5A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11720524 |
| dbSNP (classic) | rs11720524 |
| ClinGen | rs11720524 |
| ebi | rs11720524 |
| HLI | rs11720524 |
| Exac | rs11720524 |
| Gnomad | rs11720524 |
| Varsome | rs11720524 |
| LitVar | rs11720524 |
| Map | rs11720524 |
| PheGenI | rs11720524 |
| Biobank | rs11720524 |
| 1000 genomes | rs11720524 |
| hgdp | rs11720524 |
| ensembl | rs11720524 |
| geneview | rs11720524 |
| scholar | rs11720524 |
| rs11720524 | |
| pharmgkb | rs11720524 |
| gwascentral | rs11720524 |
| openSNP | rs11720524 |
| 23andMe | rs11720524 |
| SNPshot | rs11720524 |
| SNPdbe | rs11720524 |
| MSV3d | rs11720524 |
| GWAS Ctlg | rs11720524 |
| GMAF | 0.2916 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20400777
] Common variants in cardiac ion channel genes are associated with sudden cardiac death
[PMID 28085969] A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.
