rs863224477
From SNPedia
| Merged into | rs397508120 |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs863224477(-;-) |
| Make rs863224477(-;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 11 |
| Position | 2570734 |
| Gene | KCNQ1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs863224477 |
| dbSNP (classic) | rs863224477 |
| ClinGen | rs863224477 |
| ebi | rs863224477 |
| HLI | rs863224477 |
| Exac | rs863224477 |
| Gnomad | rs863224477 |
| Varsome | rs863224477 |
| LitVar | rs863224477 |
| Map | rs863224477 |
| PheGenI | rs863224477 |
| Biobank | rs863224477 |
| 1000 genomes | rs863224477 |
| hgdp | rs863224477 |
| ensembl | rs863224477 |
| geneview | rs863224477 |
| scholar | rs863224477 |
| rs863224477 | |
| pharmgkb | rs863224477 |
| gwascentral | rs863224477 |
| openSNP | rs863224477 |
| 23andMe | rs863224477 |
| SNPshot | rs863224477 |
| SNPdbe | rs863224477 |
| MSV3d | rs863224477 |
| GWAS Ctlg | rs863224477 |
| Status | Merged into rs397508120 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs863224477(G;G) |
| Significance | Pathogenic |
| Disease | Long QT syndrome |
| Variation | info |
| Gene | KCNQ1 |
| CLNDBN | Long QT syndrome |
| Reversed | 0 |
| HGVS | NC_000011.9:g.2591964delG |
| CLNSRC | |
| CLNACC | RCV000196205.1, |
