Table 1.
Disease | Genes (yield, %) |
---|---|
Long QT syndrome | KCNQ1 (30–35), KCNH2 (25–30), SCN5A (5–10) [25] |
Catecholaminergic Polymorphic Ventricular Tachycardia | RYR2 (60–65),CASQ2 (<5) [47], [49] |
Brugada Syndrome | SCN5A (20) [60] |
Hypertrophic cardiomyopathy | MYBPC3 (30–40), MYH7 (20–30), TNNT2 (10), TNNI3 (7) [66] |
Dilated cardiomyopathy | TTN (~25) [80] |
Arrhythmogenic right ventricular dysplasia/cardiomyopathy | PKP2 (46), PLN (5) [62] |