SHORT QT SYNDROME: CLINICAL EXOME PANEL (Sec. & CNVs) – 8 genes
LabGenetics
Delivery time
3-4 weeks
Sample
Blood
The Short QT Syndrome (SQTS) panel analyzes eight genes associated with this inherited cardiac channelopathy, characterized by an abnormally shortened QT interval, predisposition to ventricular tachyarrhythmias, atrial fibrillation, and a risk of sudden death. Using next-generation sequencing (NGS) with detection of SNVs, indels, and CNVs, it identifies variants in genes encoding potassium and calcium ion channels responsible for accelerating cardiac repolarization. Genes included are: KCNH2, KCNJ2, KCNQ1, CACNA1C, CACNB2, CACNA2D1, CACNA1D, and SLC22A5. For a complete list of genes included in the panel, please contact Genotica.
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