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Dementia, young onset (gene panel)

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Full name:
Dementia, young onset (gene panel)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis
Specimen:
DNA,
Peripheral (whole) blood on EDTA
Method category:
Whole Exome Sequencing (WES)
Sequence analysis: entire coding region
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Medische Genetica - UZ Antwerpen
RIZIV code:
565493-565504
Turnaround time (maximum):
6 months
Created:
14 Dec 2022 - 12:54
Changed:
19 Dec 2023 - 15:46
  • Dementia, young onset (gene panel)
    Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments
    APOE 100.00 1
    APP 100.00 1
    CHCHD10 100.00 1
    CHMP2B 100.00 1
    CSF1R 100.00 1
    FUS 100.00 1
    GRN 100.00 1
    HTRA1 95.00 1
    ITM2B 100.00 1
    MAPT 100.00 1
    NOTCH3 98.00 1
    OPTN 100.00 1
    PRNP 100.00 1
    PSEN1 100.00 1
    PSEN2 100.00 1
    TARDBP 100.00 1
    TBK1 100.00 1
    TREM2 100.00 1
    TYROBP 100.00 1
    UBQLN2 100.00 1
    VCP 100.00 1