Jak2 Exon 12 Mutation Detection

JAK2 Exon 12 mutation testing helps diagnose myeloproliferative disorders, including polycythemia vera. It is used to identify specific mutations associated with these conditions.

Also known asJak2 Exon 12 Mutation Jak2 Exon 12 Mutation

Available via

Home Collection, Lab Visit

Contains

2 parameters

Earliest reports in

7 Working Days

Test details

Jak2 Exon 12 Mutation Detection Test in Vadodara Overview

Preparations

No special preparations needed

Test included
Jak2 Exon 12 Mutation Detection includes 2 parameters

  • Specimen Source
  • Jak2 Exon 12 Mutation
Frequently Asked Questions

This molecular test detects mutations in exon 12 of the JAK2 gene, which are associated with certain myeloproliferative disorders.

It helps diagnose polycythemia vera and related conditions in patients who are negative for the more common JAK2 V617F mutation.

A blood or bone marrow sample is analyzed using PCR and sequencing methods to detect mutations.

A positive result indicates a mutation in exon 12 of JAK2, supporting a diagnosis of a myeloproliferative neoplasm.

No preparation is required. A clinical evaluation is essential for interpretation.

Test code

RD1310

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Bone MarrowOthers10
Edta Whole BloodLavender Vacutainer10

Specimen stability information

Bone Marrow, Edta Whole Blood

Collection instructions

Clinical History In Specified Format

Specimen rejection criteria

Test run frequency

Every Day TIME - 09:30

Turn around time

7 Working Days

Performing locations

Department

  • Advanced Molecular Diagnostics R&d

CPT and Loinc codes

Jak2 Exon 12 Mutation Detection

6500