CARDIAC CONDUCTION DISORDERS: CLINICAL EXOME PANEL (Sec. & CNVs) – 41 genes
LabGenetics
Delivery time
3-4 weeks
Sample
Blood
The Cardiac Conduction Disorders panel analyzes 41 genes involved in hereditary alterations of the cardiac electrical conduction system, responsible for atrioventricular blocks, sinus dysfunction, arrhythmias and risk of sudden death.
Through massive sequencing (NGS) with detection of SNVs, indels and CNVs, it is possible to identify variants in genes that encode ion channels, cytoskeleton proteins, sarcomere proteins and intercellular coupling proteins.
Featured genes: SCN5A, LMNA, NKX2-5, TBX5, PRKAG2, TRPM4, DES, DSP, GJA5, PKP2.
You can consult the complete list of genes included in the panel by contacting Genotica.
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