Genomic Unity® Cardiac Channelopathies Analysis

Genomic Unity® Cardiac Channelopathies Analysis is an appropriate test for individuals with or suspected of having insufficiency or hyperactivity of the cardiac ion channels.

Order this test when the patient presents with symptoms of cardiac channelopathies, and you'd like the option to reflex up to Genomic Unity® Whole Genome Analysis.

  • Sequencing analysis of cardiac channelopathy genes
  • Del/dup analysis of cardiac channelopathy genes

Optionally includes:

  • Reflex to Genomic Unity® Whole Genome Analysis or Genomic Unity® Exome Analysis

ANK2, CASQ2, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, RYR2, SCN5A

 
Disorders that can be tested for include: Atrial fibrillation Brugada syndrome Hypertrophic cardiomyopathy Idiopathic ventricular fibrillation Jervell and Lange-Nielsen syndrome Long QT syndrome Romano-Ward syndrome Short QT syndrome

SNVs and Indels up to 50bp
99.7% sensitivity
99.6% positive predictive value

Structural variants:
96% clinical sensitivity

81403, 81404, 81405, 81406, 81407, 81479

The CPT codes provided are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

Blood - 5ml
Saliva - contact us for a kit
gDNA - 5μg

Turn around time is 6-8 weeks from sample receipt.