KCNE1 - long QT syndrome ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Long QT syndrome

This product is also part of the following panels:

  • Arrhythmia and cardiac conduction disorders panel¹
  • Comprehensive preconception carrier test panel¹
  • Hearing impairment panel (including GJB2)
  • Heart disorders panel¹
  • Long QT syndrome panel¹
  • Mendelian inherited disorders panel
  • panel Arrhythmia targeting (13 genes) - LQT, SQT, BrS, CPVT, SSS ¹
  • panel Jervell and Lange-Nielsen syndrome (KCNQ1, KCNE1) ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries

OMIM: 176261
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 353

Exome

Arrhythmia and cardiac conduction disorders panel¹

Turnaround time
8 weeks
Performing laboratory
Maastricht UMC+
€ 750

Arrhythmia and cardiac conduction disorders panel¹




€ 750

Arrhythmia and cardiac conduction disorders panel¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Long QT syndrome
  • Conditions > Cardiovascular > Short QT syndrome
  • Conditions > Cardiovascular > Sick sinus syndrome

Turnaround time
8 weeks

Method

  • Exome analysis (WES or WGS data)
Remarks
This test is inclusive panelwide CNV analysis. Upon request a genomewide CNV analysis can be performed.

Panel version: DG 3.8.1
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood (preferably), isolated DNA (only when EDTA blood is not an option)





€ 750
Exome

Long QT syndrome panel¹

Turnaround time
8 weeks
Performing laboratory
Maastricht UMC+
€ 750

Long QT syndrome panel¹




€ 750

Long QT syndrome panel¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Long QT syndrome
  • Conditions > Cardiovascular > Short QT syndrome
  • Conditions > Cardiovascular > Sick sinus syndrome

Turnaround time
8 weeks

Method

  • Exome analysis (WES or WGS data)
Remarks
This test is inclusive panelwide CNV analysis. Upon request a genomewide CNV analysis can be performed.

Panel version: DG 3.8.1
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood (preferably), isolated DNA (only when EDTA blood is not an option)





€ 750
Panel

panel Arrhythmia targeting (13 genes) - LQT, SQT, BrS, CPVT, SSS ¹

Turnaround time
8 weeks
Performing laboratory
Maastricht UMC+
€ 618

panel Arrhythmia targeting (13 genes) - LQT, SQT, BrS, CPVT, SSS ¹



€ 618

panel Arrhythmia targeting (13 genes) - LQT, SQT, BrS, CPVT, SSS ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Arrhythmogenic right ventricular cardiomyopathy (ARVD)
  • Conditions > Cardiovascular > Brugada syndrome
  • Conditions > Cardiovascular > Long QT syndrome
  • Conditions > Cardiovascular > Short QT syndrome
  • Conditions > Cardiovascular > Sick sinus syndrome

Turnaround time
8 weeks

Method

  • Sequence analysis of all coding exons and flanking intron-exon boundaries
Remarks
It includes sequencing of all coding regions of the following 13 genes: CACNA1C, CALM1, CASQ2, HCN4, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1, LMNA, RYR2, SCN5A en TRDN.

Performing laboratory: Maastricht UMC+
Authorized material(s): FFPE




€ 618