KCNQ1 - familial atrial fibrillation ¹

This test is available for the following conditions:

  • Conditions > Cardiovascular > Familial atrial fibrillation

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 Jervell and Lange-Nielsen syndrome (KCNQ1, KCNE1) ¹
  • panel short QT syndrome (CACNA1C (ex 8), KCNQ1, KCNH2, KCNJ2) ¹
  • WES comprehensive preconception carrier test ¹
  • WES hearing impairment (95.3% **)
  • WES heart disorders¹ (95.3% **)
  • WES Mendelian inherited disorders (95.3% **)

** % 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: 607542
Performing laboratory: Maastricht UMC+
Authorized material(s): EDTA blood, Isolated DNA, Buccal mucous membrane




€ 476

Gene

KCNQ1 - familial atrial fibrillation ¹

Turnaround time
Complete analysis: 8 weeks / Targeted analysis: 4 weeks
Performing laboratory
Maastricht UMC+
€ 476

KCNQ1 - familial atrial fibrillation ¹



€ 476