KCNQ1
| Deellabo: | PGD DNA |
| Gen (Gen Code): | KCNQ1 |
| Aliases Gen: | LQT; RWS; WRS; LQT1; SQT2; ATFB1; ATFB3; JLNS1; KCNA8; KCNA9; Kv1.9; Kv7.1; KVLQT1; FLJ26167; KCNQ1 |
| Gen ID (NCBI): | 3784 |
| OMIM Gen ID: | 607542 |
| Chromosomale locatie: | 11p15.5-p15.4 |
| Genetische aandoening / Analyse: | Long QT syndroom 1 (LQT1) |
| OMIM aandoening ID: | 192500 |
| Overerving: | AD |
| Aliases aandoening: | LONG QT SYNDROME 1; LQT1 WARD-ROMANO SYNDROME; WRS ROMANO-WARD SYNDROME; RWS VENTRICULAR FIBRILLATION WITH PROLONGED QT INTERVAL |