Number of Panel Genes: 
25

Brugada syndrome is a cardiac channelopathy characterized by specific ECG abnormalities such as ST-segment elevation in the right precordial leads and incomplete right bundle-branch block. Typical findings include ventricular fibrillation, syncope and cardiac arrest. Brugada syndrome is associated with high risk of sudden cardiac death in otherwise healthy young adults. The age-of-onset is usually in the adulthood.read more

Tests Available

25 Panel Genes: ABCC9, ANK2, CACNA1C, CACNA2D1, CACNB2, CAV3, FGF12, GPD1L, HCN4, KCND2, KCND3, KCNE3, KCNE5, KCNH2, KCNJ8, PKP2, RANGRF, SCN1B, SCN2B, SCN3B, SCN5A, SCN10A, SEMA3A, SLMAP, TRPM4
Next Generation Sequencing
$1,495
Test Code: 5315
Deletion / Duplication
$990
Test Code: 5316
NGS/Del Dup Comprehensive
$1,870
Test Code: 5317

Test Details

Technical Information
Panel Genes: 
ABCC9, ANK2, CACNA1C, CACNA2D1, CACNB2, CAV3, FGF12, GPD1L, HCN4, KCND2, KCND3, KCNE3, KCNE5, KCNH2, KCNJ8, PKP2, RANGRF, SCN1B, SCN2B, SCN3B, SCN5A, SCN10A, SEMA3A, SLMAP, TRPM4
Disease Groups: 
Cardiovascular Disorders
Billing
Price: 
$1,495
CPT Codes: 
81403 x 1
81404 x 2
81406 x 3
81407 x 1
81479 x 18
Ordering
SKU:
5315
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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