Number of Panel Genes: 
6

Short QT syndrome (SQT) is an inherited channelopathy of the heart characterized by a short QT interval. It is associated with syncope, atrial and ventricular tachyarrhythmias in the absence of structural heart disease, and increased risk of sudden cardiac death. Patients are typically young, but SQT can manifest at any age.

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Tests Available

6 Panel Genes: CACNA1C, CACNA2D1, CACNB2, KCNH2, KCNJ2, KCNQ1
Next Generation Sequencing
$1,120
Test Code: 5330
Deletion / Duplication
$990
Test Code: 5331
NGS/Del Dup Comprehensive
$1,495
Test Code: 5332

Test Details

Technical Information
Panel Genes: 
CACNA1C, CACNA2D1, CACNB2, KCNH2, KCNJ2, KCNQ1
Disease Groups: 
Cardiovascular Disorders
Billing
Price: 
$1,120
CPT Codes: 
81403 x 1
81406 x 3
81479 x 2
Ordering
SKU:
5330
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: 
  1. Whole blood: purple-top (EDTA) tube, minimum of 3 ml
  2. Genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl)
  3. Fibroblasts: 4 confluent T-25 flasks
  4. Saliva: only samples collected in Oragene DNA Self-Collection Kit or Oragene Saliva Collection Kit for Young Children are accepted
Prenatal Specimens: 
  1. Cultured cells: 4 confluent T-25 flasks derived from amnio or CVS samples
  2. 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.

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