Genes | ABCC9, AKAP9, ANK2, ASPH, CACNA1C, CACNA1D, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, DPP6 (c.-340C>T NM_001936), GJA5, GPD1L, HCN4, JPH2, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNE5(KCNE1L), KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LAMP2, LMNA, NPPA, PKP2, PLN, PRAKG2, RANGSF(MOG1), RYR2, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SLMAP, SNTA1, TNNT2, TRDN, TRPM4 |
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Lab method | NGS Sequencing & Del/Dup Analysis |
Turnaround time | 3 months |
Location | Location AMC |
Price | € 1.095,00 |
AGDx NGS – Arrhythmia panel plus CNV
Test code: D00481Disorder(s)
- Atrial Fibrillation
- Atrial Standstill (OMIM: 108770)
- Brugada Syndrome
- Cardiac Arrhythmia
- Catecholaminergic Polymorphic Ventricular Tachycardia - CPVT
- Conduction Defects
- Idiopathic Ventricular Fibrillation
- Long QT Syndrome - LQT
- Paroxysmal Ventricular Fibrillation (OMIM: 603829)
- Short QT Syndrome
- Sick Sinus Syndrome