rs770047651
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs770047651(C;T) |
| Make rs770047651(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 7 |
| Position | 150957291 |
| Gene | KCNH2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs770047651 |
| dbSNP (classic) | rs770047651 |
| ClinGen | rs770047651 |
| ebi | rs770047651 |
| HLI | rs770047651 |
| Exac | rs770047651 |
| Gnomad | rs770047651 |
| Varsome | rs770047651 |
| LitVar | rs770047651 |
| Map | rs770047651 |
| PheGenI | rs770047651 |
| Biobank | rs770047651 |
| 1000 genomes | rs770047651 |
| hgdp | rs770047651 |
| ensembl | rs770047651 |
| geneview | rs770047651 |
| scholar | rs770047651 |
| rs770047651 | |
| pharmgkb | rs770047651 |
| gwascentral | rs770047651 |
| openSNP | rs770047651 |
| 23andMe | rs770047651 |
| SNPshot | rs770047651 |
| SNPdbe | rs770047651 |
| MSV3d | rs770047651 |
| GWAS Ctlg | rs770047651 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs770047651(T;T) |
| Alt | rs770047651(T;T) |
| Reference | Rs770047651(C;C) |
| Significance | Probable-Pathogenic |
| Disease | Long QT syndrome not provided |
| Variation | info |
| Gene | KCNH2 |
| CLNDBN | Long QT syndrome not provided |
| Reversed | 0 |
| HGVS | NC_000007.13:g.150654379C>T |
| CLNSRC | |
| CLNACC | RCV000200566.3, RCV000223833.1, |
