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JAK2 Gene Leukemia, acute myelogenous NGS Genetic Test

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JAK2 Gene Leukemia, acute myelogenous NGS Genetic Test

Short Name: JAK2 AML NGS

Also known as: JAK2 Mutation Analysis, JAK2 NGS Panel, Acute Myelogenous Leukemia Genetic Test

JAK2 Gene Leukemia, acute myelogenous NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in Reports are typically delivered within 3 to 4 weeks after sample receipt.. Free home collection in 300+ cities across India.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of this test is to detect JAK2 gene mutations in patients suspected of having acute myelogenous leukemia or related myeloproliferative disorders. It helps in confirming diagnosis, assessing disease severity, guiding targeted therapy, and monitoring treatment response. NGS technology allows simultaneous analysis of multiple genes, providing a comprehensive mutational profile.

Test Code
5995
CPT Code
81445
ICD Code
C92.00
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Reports are typically delivered within 3 to 4 weeks after sample receipt.
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

No special preparation required. Inform your doctor about any medications or supplements you are taking.

Method: Venipuncture or FTA card spot

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in your arm. If using FTA card, a drop of blood will be placed on the card.

Step 3

Report Delivery

You can resume normal activities immediately. No restrictions.

Timeline: Reports are typically delivered within 3 to 4 weeks after sample receipt.

Patient Instructions

1
Before the Test:No special preparation required. Inform your doctor about any medications.
2
During the Test:A blood sample is drawn. The procedure is quick and minimally invasive.
3
After the Test:You can resume normal activities. Results will be available in 3-4 weeks.

About This Test

Who Should Get This Test

The purpose of this test is to detect JAK2 gene mutations in patients suspected of having acute myelogenous leukemia or related myeloproliferative disorders. It helps in confirming diagnosis, assessing disease severity, guiding targeted therapy, and monitoring treatment response. NGS technology allows simultaneous analysis of multiple genes, providing a comprehensive mutational profile.

How to Prepare

  • For blood sample: Use EDTA vacutainer, fill to indicated mark, mix gently.
  • For FTA card: Apply blood drops to the designated circles, air dry for 30 minutes.
  • Label the sample with patient name, date, and time of collection.
  • Transport sample to the lab at ambient temperature within 24 hours.

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"JAK2 mutations are critical in myeloproliferative neoplasms and AML. NGS provides comprehensive detection of JAK2 and associated mutations, guiding targeted therapy and prognosis."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 mL blood or 2-3 drops on FTA card
ContainerEDTA vacutainer or FTA card
Collection MethodVenipuncture or FTA card spot

Sample Stability

Blood: 24 hours at room temperature, 7 days at 2-8°C
Extracted DNA: 1 week at -20°C
FTA card: Stable for months at room temperature
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Improper labeling
  • Sample received after prolonged transit time

Understanding Your Results

The test report will indicate whether JAK2 mutations are detected or not. If a mutation is found, the specific variant and its clinical significance will be described.
📊

JAK2 V617F Positive

Indicates presence of JAK2 mutation, commonly associated with myeloproliferative neoplasms and some AML cases. May guide targeted therapy.

📊

JAK2 Exon 12 Positive

Rare mutation, also associated with myeloproliferative disorders. Clinical significance similar to V617F.

📊

No JAK2 Mutation Detected

No mutation in JAK2 gene found. Other genetic causes should be considered.

⚠️ When to Consult a Doctor:

Consult your oncologist if you experience persistent fatigue, unexplained fever, easy bruising, or abnormal blood counts. Early diagnosis and treatment are crucial.

Limitations

  • NGS may not detect very large deletions or rearrangements
  • Mutations in genes not covered by the panel will not be identified
  • Results should be interpreted in conjunction with clinical and pathological findings
  • Low-level mutations may be below detection limit

Risks & Considerations

  • Minimal risk of bleeding or bruising at the puncture site
  • Slight dizziness or fainting during blood draw

Interfering Factors

  • Clotted or hemolyzed blood samples may affect DNA quality
  • Insufficient DNA quantity or quality
  • Recent blood transfusion may dilute patient's cells
  • Contamination during sample collection

Compare With Similar Tests

TestJAK2 Gene Leukemia, acute myelogenous NGS Genetic TestJAK2 V617F PCRJAK2 Exon 12 PCRBone Marrow Biopsy
ComparisonJAK2 Gene Leukemia, acute myelogenous NGS Genetic TestTargeted PCR detects only V617F mutation, while NGS covers multiple exons and other genes.PCR for exon 12 only, less comprehensive than NGS.Invasive procedure, provides morphological and genetic information, but NGS is non-invasive and more sensitive.

Frequently Asked Questions

What is the JAK2 gene and how is it related to leukemia?
The JAK2 gene provides instructions for making a protein that regulates cell growth and division. Mutations in JAK2 can lead to uncontrolled cell growth, contributing to leukemia, especially myeloproliferative neoplasms and some AML cases.
What is the cost of the JAK2 Gene Leukemia NGS Genetic Test at DNA Labs India?
The test costs INR 20,000. This includes home sample collection, genetic counseling, NGS analysis, and a comprehensive clinical report with raw data files.
What sample is required for this test?
The sample can be blood (5 mL in EDTA tube), extracted DNA, or one drop of blood on an FTA card. Home collection is available for online bookings.
How long does it take to get the results?
Reports are typically available within 3 to 4 weeks after the sample is received at the laboratory.
Is fasting required before the test?
No, fasting is not required for this test. You can eat and drink normally before sample collection.
What does NGS technology mean?
Next-generation sequencing (NGS) is a high-throughput method that can sequence multiple genes simultaneously, allowing comprehensive detection of mutations in JAK2 and other related genes.
Will I receive raw data files with my report?
Yes, DNA Labs India is transparent and provides raw data files (FASTQ, VCF) along with the clinical report for verification and further analysis.
Can this test detect all JAK2 mutations?
The NGS panel covers common JAK2 mutations including V617F and exon 12-15 mutations. However, very rare mutations may not be detected. It is important to discuss with your doctor.
What is the difference between this NGS test and a regular PCR test?
PCR tests target specific mutations like V617F, while NGS analyzes multiple genes and exons, providing a broader mutational profile and higher sensitivity.
Is home sample collection available in my city?
Yes, we offer free home sample collection across major cities in India including Mumbai, Delhi, Bangalore, Hyderabad, and many more. Please check the list or contact us.
How should I prepare for the test?
No special preparation is needed. Inform your doctor about any medications you are taking. The sample collection is quick and simple.
What is the clinical significance of a positive JAK2 mutation result?
A positive result indicates the presence of a JAK2 mutation, which can help confirm a diagnosis, guide treatment options (e.g., JAK inhibitors), and provide prognostic information.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.

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Your medical data is protected under Indian law.

Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.

DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.

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