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Amyloidosis hereditary (gene panel)

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Full name:
Amyloidosis hereditary (gene panel)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Mutation confirmation,
Post-natal Diagnosis,
Predictive and Pre-symptomatic diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centre de Génétique Humaine - Erasme ULB
RIZIV code:
565456-565460
Turnaround time (maximum):
3 months
Document(s):
Created:
13 Dec 2019 - 12:30
Changed:
17 Aug 2023 - 10:38
URL:
https://ulbgenetics.be/compendium-des-analyses/#GM04
  • Amyloidosis (3 genes) - ULB
    Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments
    TTR 100.00 -2
    APOA1 100.00 -2
    APOA2 100.00 -2