Beta-globin hemoglobinopathies, Hemoglobinopathy C (HbC) (HBB hot spot mutation - p.Glu6Lys)

Genetic test Export to PDF
Full name:
Beta-globin hemoglobinopathies, Hemoglobinopathy C (HbC) (HBB hot spot mutation - p.Glu6Lys)
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Carrier diagnosis,
Mutation confirmation,
Post-natal Diagnosis,
Pre-implantation genetic diagnosis,
Prenatal diagnosis
Specimen:
Peripheral (whole) blood on EDTA,
Amniotic fluid,
Chorionic villi,
Cell culture
Method category:
Method technique:
Laboratory:
RIZIV code:
EQA:
  • 2015 DNA Sequencing - Sanger EMQN
  • 2016 DNA Sequencing - Sanger EMQN
  • 2017 DNA Sequencing - Sanger EMQN
  • 2018 DNA Sequencing - Sanger EMQN
  • 2019 DNA Sequencing - Sanger EMQN
  • 2021 DNA Sequencing - Sanger EMQN
  • 2022 DNA Sequencing - Sanger EMQN
Accreditation (ISO 15189):
2021-10-07 / 2026-06-14
Turnaround time (maximum):
2 months (10 working days for prenatal diagnosis)
Document(s):
Created:
23 Aug 2019 - 16:28
Changed:
01 Mar 2023 - 16:28
URL: