SCN1B - Brugada syndrome ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Brugada syndrome

This product is also part of the following panels:

  • panel Arrhythmia targeting (27 genes) - LQT, SQT, BrS, CPVT, SSS ¹
  • panel cardiomyopathy (27 genes) - HCM, DCM, ARVD/C, RCM ¹
  • panel small fiber neuropathy (SCN3A,SCN7A,SCN8A,SCN9A,SCN10A,SCN11A,SCN1B,SCN2B,SCN3B,SCN4B,GLA) ¹
  • WES comprehensive preconception carrier test ¹
  • WES epilepsy (98.1% **)
  • WES heart disorders¹ (98.1% **)
  • WES intellectual disability (98.1% **)
  • WES Mendelian inherited disorders (98.1% **)

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

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

OMIM: 600235
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 360

Panel

panel Arrhythmia targeting (27 genes) - LQT, SQT, BrS, CPVT, SSS ¹

Turnaround time
8 weeks
Performing laboratory
Maastricht UMC+
€ 618

panel Arrhythmia targeting (27 genes) - LQT, SQT, BrS, CPVT, SSS ¹



€ 618

panel Arrhythmia targeting (27 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 27 genes ABCC9, AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CALM1, CASQ2, CAV3, DPP6, GPD1L, HCN4, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ8, KCNQ1, LMNA, RYR2, SCN1B, SCN3B, SCN5A, SNTA1, TNNT2, TRDN.

Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA




€ 618
Gene

SCN1B - Brugada syndrome ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 360

SCN1B - Brugada syndrome ¹



€ 360
Gene

SCN5A - Brugada syndrome ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 583

SCN5A - Brugada syndrome ¹



€ 583

SCN5A - Brugada syndrome ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Brugada syndrome

This product is also part of the following panels:

  • panel Arrhythmia targeting (27 genes) - LQT, SQT, BrS, CPVT, SSS ¹
  • panel cardiomyopathy (27 genes) - HCM, DCM, ARVD/C, RCM ¹
  • panel cardiomyopathy core targeting (46 genen) - HCM, DCM, ARVD/C, RCM ¹
  • panel sick sinus syndrome (SCN5A, HCN4) ¹
  • WES heart disorders¹ (99.0% **)
  • WES Mendelian inherited disorders (99.0% **)

** % of the coding region of this gene has a coverage of >20x. (Without % information : This is a non-coding gene for which coverage statistics could not be determined)

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

Method

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

OMIM: 600163
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 583