rs9388451
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs9388451(C;C) |
| Make rs9388451(C;T) |
| Make rs9388451(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 125769231 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs9388451 |
| dbSNP (classic) | rs9388451 |
| ClinGen | rs9388451 |
| ebi | rs9388451 |
| HLI | rs9388451 |
| Exac | rs9388451 |
| Gnomad | rs9388451 |
| Varsome | rs9388451 |
| LitVar | rs9388451 |
| Map | rs9388451 |
| PheGenI | rs9388451 |
| Biobank | rs9388451 |
| 1000 genomes | rs9388451 |
| hgdp | rs9388451 |
| ensembl | rs9388451 |
| geneview | rs9388451 |
| scholar | rs9388451 |
| rs9388451 | |
| pharmgkb | rs9388451 |
| gwascentral | rs9388451 |
| openSNP | rs9388451 |
| 23andMe | rs9388451 |
| SNPshot | rs9388451 |
| SNPdbe | rs9388451 |
| MSV3d | rs9388451 |
| GWAS Ctlg | rs9388451 |
| GMAF | 0.4605 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23872634 ]
|
| Trait | Brugada syndrome |
| Title | Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. |
| Risk Allele | C |
| P-val | 5E-17 |
| Odds Ratio | 1.58 [1.42-1.75] |
[PMID 28085969] A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.
[PMID 32490690] Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated with Brugada Syndrome: SADS-TW BrS Registry.
