Number of Panel Genes:
41
Cardiac channelopathies encompasses disorders that affect cardiac conduction. They include Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, long QT syndrome, and short QT syndrome. They are characterized by malignant arrhythmias and a high risk of sudden cardiac death in individuals without under laying structural heart disease.
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41 Panel Genes: ABCC9, AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, FGF12, GPD1L, HCN4, KCND2, KCND3, KCNE1, KCNE2, KCNE3, KCNE5, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, PKP2, NOS1AP, RANGRF, RYR2, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SCN10A, SEMA3A, SLMAP, SNTA1, TECRL, TRDN, TRPM4
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Next Generation Sequencing
$1,400
Test Code: 5318
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Deletion / Duplication
$990
Test Code: 5319
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NGS/Del Dup Comprehensive
$1,600
Test Code: 5320
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Test Details
Technical Information
Panel Genes:
ABCC9, AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, FGF12, GPD1L, HCN4, KCND2, KCND3, KCNE1, KCNE2, KCNE3, KCNE5, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, PKP2, NOS1AP, RANGRF, RYR2, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SCN10A, SEMA3A, SLMAP, SNTA1, TECRL, TRDN, TRPM4
Disease Groups:
Cardiovascular Disorders
Billing
CPT Codes:
81413 x 1
Ordering
SKU:
5318 Turnaround Time:
Typically 2 to 4 weeks from receipt of a sample in the laboratory. All cases involving ongoing pregnancies will be expedited.
Non-Prenatal Specimens:
- Whole blood: purple-top (EDTA) tube, minimum of 3 ml
- Genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl)
- Fibroblasts: 2 confluent T-25 flasks
- Saliva: only samples collected in Oragene DNA Self-Collection Kit or Oragene Saliva Collection Kit for Young Children are accepted
Prenatal Specimens:
- Cultured cells: 2 confluent T-25 flasks derived from amnio or CVS samples
- Genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl)
Shipping:
Ship all specimen types at room temperature by overnight courier. Do not freeze.