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ABS019 : THE IMPORTANCE OF GENETIC VARIANT DATABASES IN INTERPRETIVE REPORTING FOR HERITABLE BLEEDING DISORDERS

Researchers

Presenter

  • I. Jennings

Principal Investigators

  • M. Hill

  • C. Millar

  • A. Page

  • M. Sutherland

  • R. Wheeler

  • S. Kitchen

  • I. Walker

Medical Centers

  • UK NEQAS (BLOOD COAGULATION), Sheffield

  • Molecular Diagnostics, Dept Clinical Pathology, Nottingham University Hospitals NHS Trust, Nottingham

  • Centre for Haematology, Imperial College Healthcare NHS Trust, London

  • Haemophilia, Thrombosis & Immunology Centre, Royal Infirmary of Edinburgh, Edinburgh

  • Manchester University NHS FT, Manchester

  • Molecular Haemostasis Laboratory, Viapath, St Thomas Hospital, London, United Kingdom

Locations

  • United Kingdom

Companies

  • N/A

Study Components

Therapeutic Area

  • Blood/haematological Diseases

Disease

  • Hemophilia

Biomarkers

  • N/A

Drug/Treatment

  • N/A

Outcome

  • N/A

Study Design

  • N/A

Phase

  • NA

Study Id's

  • N/A

Sponsors

  • N/A

Result

  • N/A

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