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GTR Home > Tests > Genetic Study of Hereditary Thrombophilia (10 genes)

Overview

Test order codeHelp: Genetic study of Hereditary Thrombophilia

Test name

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Genetic Study of Hereditary Thrombophilia (10 genes) (TromboGene)

Purpose of the test

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This is a clinical test intended for Help: Diagnosis, Mutation Confirmation, Risk Assessment, Screening

Condition

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How to order

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Order URL Help: http://www.heartgenetics.com/order-a-test/

Specimen source

Buccal swab
Dried blood spot (DBS) card
Fresh tissue
Isolated DNA
Paraffin block
Peripheral (whole) blood
Saliva

Methodology

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Molecular Genetics
ESequence analysis of select exons
High Resolution Melting
  • Other
TTargeted variant analysis
Allele-specific primer extension (ASPE)
  • MassARRAY┬« System by Agena Bioscience
  • Other

Summary of what is tested

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Clinical utility

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Not provided

Clinical validity

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Not provided

Test services

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  • Clinical Testing/Confirmation of Mutations Identified Previously, Order code: TromboGene
  • Custom mutation-specific/Carrier testing, Order code: TromboGene

Practice guidelines

  • NICE, 2020
    UK NICE Guideline NG158, Venous thromboembolic diseases: diagnosis, management and thrombophilia testing, 2020

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.