rs10428132
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10428132(G;G) |
| Make rs10428132(G;T) |
| Make rs10428132(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 38736063 |
| Gene | SCN10A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10428132 |
| dbSNP (classic) | rs10428132 |
| ClinGen | rs10428132 |
| ebi | rs10428132 |
| HLI | rs10428132 |
| Exac | rs10428132 |
| Gnomad | rs10428132 |
| Varsome | rs10428132 |
| LitVar | rs10428132 |
| Map | rs10428132 |
| PheGenI | rs10428132 |
| Biobank | rs10428132 |
| 1000 genomes | rs10428132 |
| hgdp | rs10428132 |
| ensembl | rs10428132 |
| geneview | rs10428132 |
| scholar | rs10428132 |
| rs10428132 | |
| pharmgkb | rs10428132 |
| gwascentral | rs10428132 |
| openSNP | rs10428132 |
| 23andMe | rs10428132 |
| SNPshot | rs10428132 |
| SNPdbe | rs10428132 |
| MSV3d | rs10428132 |
| GWAS Ctlg | rs10428132 |
| GMAF | 0.2957 |
| Max Magnitude | 0 |
| ? | (G;G) (G;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 | T |
| P-val | 1E-68 |
| Odds Ratio | 2.55 [2.30-2.84] |
[PMID 32490690] Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated with Brugada Syndrome: SADS-TW BrS Registry.
