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JAK2 Mutation Analysis in Myeloproliferative Disorders

JAK2 mutation analysis utilizes genomic DNA isolated from a patient’s sample in a real-time PCR assay to detect the V617F point mutation in the JAK2 gene. This assay has been validated to detect a minimum of 1% mutant sequence in a background of normal sequence. Identification of this point mutation in the JAK2 gene now allows for reliable diagnosis, classification and potential treatment of patients with myeloproliferative disorders (MPD).

Information Sheet - JAK2 Mutation Analysis (PDF)

CPT Codes:

83891(1), 83892(1), 83896(2), 83898(1), 83912(1)


Specimen Requirements:
  1. Peripheral Blood:
    • 1-5 ml in an EDTA (lavender-top) tube.
  2. Bone Marrow Aspirate:
    • 2-3 ml in an EDTA (lavender-top) tube.

Turnaround Time:

4-6 days


Client Services: Oncology/Pathology   800-447-5816

Specimen Services/Pickup:  877-246-1226