Long QT Syndrome (KCNQ1, KCNH2, KCNE1;MLPA)
Clinical Genetic Test
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offered by
GTR Test Accession: Help GTR000519796.1
INHERITED DISEASECARDIOVASCULARDYSMORPHOLOGY ... View more
Registered in GTR: 2014-11-10
Last annual review date for the lab: 2023-12-11 LinkOut
At a Glance
Diagnosis
Long QT syndrome 1; Long QT syndrome 2; Long QT syndrome 5
Genes (3): Help
KCNE1 (21q22.12); KCNH2 (7q36.1); KCNQ1 (11p15.5-15.4)
Molecular Genetics - Deletion/duplication analysis: Multiplex Ligation-dependent Probe Amplification (MLPA)
Not provided
Not provided
Not provided
Ordering Information
Offered by: Help
MVZ Dr. Eberhard & Partner Dortmund
View lab's website
Test Order Code: Help
LQTM
Pre-test genetic counseling required: Help
Not provided
Post-test genetic counseling required: Help
Not provided
Recommended fields not provided:
Conditions Help
Total conditions: 3
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 3
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Deletion/duplication analysis
Multiplex Ligation-dependent Probe Amplification (MLPA)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Analytical sensitivity and specificity >99%
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

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