List of diseases covered by Arrhythmia NGS panel

Gene Condition
ABCC9 Atrial fibrillation, familial, 12; Dilated cardiomyopathy 1O
AKAP9 Long QT syndrome 11
ANK2 Cardiac arrhythmia, ankyrin B-related
CACNA1C Brugada syndrome 3
CACNB2 Brugada syndrome 4
CASQ2 Ventricular tachycardia, catecholaminergic polymorphic, 2
CAV3 Familial hypertrophic cardiomyopathy 1; Long QT syndrome 9
DES Dilated cardiomyopathy 1I
DSC2 Arrhythmogenic right ventricular cardiomyopathy, type 11
DSG2 Arrhythmogenic right ventricular cardiomyopathy, type 10;
Dilated cardiomyopathy 1BB
DSP Arrhythmogenic right ventricular cardiomyopathy, type 8;
Cardiomyopathy dilated with woolly hair and keratoderma;
Cardiomyopathy, dilated, with woolly hair, keratoderma,
and tooth agenesis
GJA5 Atrial fibrillation, familial, 11; Atrial standstill 1
GPD1L Brugada syndrome 2
HCN4 Brugada syndrome 8;
Sick sinus syndrome 2, autosomal dominant
JUP Arrhythmogenic right ventricular cardiomyopathy, type 12;
Naxos disease
KCNA5 Atrial fibrillation, familial, 7
KCND3 Brugada syndrome 9
KCNE1 Long QT syndrome 5;
Jervell and Lange-Nielsen syndrome 2
KCNE2 Atrial fibrillation, familial, 4;
Long QT syndrome 6
KCNE3 Brugada syndrome 6
KCNH2 Long QT syndrome 2; Short QT syndrome 1
KCNJ2 Andersen Tawil syndrome;
Atrial fibrillation, familial, 9; Short QT syndrome 3
KCNJ8 Cantu syndrome, KCNJ8 related
KCNQ1 Atrial fibrillation, familial, 3;
Jervell and Lange-Nielsen syndrome 1; Long QT syndrome 1;
Short QT syndrome 2
LMNA Dilated cardiomyopathy 1A
NKX2-5 Atrial septal defect 7 with or without
atrioventricular conduction defect;
Conotruncal heart malformations; Hypoplastic left heart syndrome 2;
Ventricular septal defect 3
NPPA Atrial fibrillation, familial, 6; Atrial standstill 2
PKP2 Arrhythmogenic right ventricular cardiomyopathy, type 9
PLN Dilated cardiomyopathy 1P; Familial hypertrophic cardiomyopathy 18
RYR2 Arrhythmogenic right ventricular dysplasia, familial, 2;
Catecholaminergic polymorphic ventricular tachycardia type 1
SCN1B Atrial fibrillation, familial, 13; Brugada syndrome 5
SCN2B Atrial fibrillation, familial, 14
SCN3B Brugada syndrome 7
SCN4B Long QT syndrome 10
SCN5A Atrial fibrillation, familial, 10; Brugada syndrome 1;
Dilated cardiomyopathy 1E; Long QT syndrome 3;
Sick sinus syndrome 1, autosomal recessive;
Paroxysmal familial ventricular fibrillation 1
SNTA1 Long QT syndrome 12
TGFB3 Arrhythmogenic right ventricular dysplasia, familial 1
TMEM43 Arrhythmogenic right ventricular cardiomyopathy, type 5