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® Exome Plus Analysis.

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

Optionally includes:

  • Reflex to Genomic Unity® Exome Plus 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.

Forms

Tests which include this analysis