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CSF3R Gene Neutrophilia, hereditary NGS Genetic Test

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CSF3R Gene Neutrophilia, hereditary NGS Genetic Test

Short Name: CSF3R Neutrophilia Genetic Test

Also known as: CSF3R Gene Mutation Test, Hereditary Neutrophilia NGS Test

CSF3R Gene Neutrophilia, hereditary 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 3 to 4 weeks. Free home collection in 300+ cities across India.

Genetic Test🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SHAILAJA RAGHUNATH MURDESHWAR

Dr SHAILAJA RAGHUNATH MURDESHWAR

Consultant Physician · Reg: 8052

Last reviewed: September 7, 2026

Overview

To identify pathogenic variants in the CSF3R gene associated with hereditary neutrophilia, aiding in diagnosis, risk assessment for blood cancers, and family planning.

Test Code
5611
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3 to 4 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Obtain clinical history and family pedigree. Genetic counseling session recommended.

Method: Venipuncture or Buccal Swab

Step 2

Laboratory Analysis

Collect blood sample via venipuncture or buccal swab.

Step 3

Report Delivery

Label and transport sample to laboratory under appropriate conditions.

Timeline: 3 to 4 weeks

Patient Instructions

1
Before the Test:Schedule a genetic counseling session to discuss the test, implications, and family history.
2
During the Test:Sample collection takes about 15-30 minutes.
3
After the Test:Wait for 3-4 weeks for results. Follow up with genetic counselor for interpretation.

About This Test

Who Should Get This Test

To identify pathogenic variants in the CSF3R gene associated with hereditary neutrophilia, aiding in diagnosis, risk assessment for blood cancers, and family planning.

How to Prepare

  • No fasting required
  • Provide detailed clinical and family history
  • Ensure sample is properly labeled

Doctor's Notes

Reviewed by — MBBS, MD (General Medicine) · Reg. No. 8052

"This genetic test is essential for identifying mutations in the CSF3R gene, which can lead to hereditary neutrophilia and increased risk of blood cancers. Early diagnosis allows for better management and monitoring."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume3-5 mL of blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or Buccal Swab

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for longer periods
Sample Rejection Criteria:
  • Hemolyzed or clotted sample
  • Insufficient sample volume
  • Improperly labeled sample

Understanding Your Results

Results are reported as the presence or absence of pathogenic variants in the CSF3R gene.
📊

Pathogenic variant detected

Confirms diagnosis of hereditary neutrophilia. Increased risk for blood cancers. Genetic counseling advised.

📊

No pathogenic variant detected

CSF3R gene mutations not found. Symptoms may be due to other causes. Further testing may be needed.

📊

Variant of uncertain significance

Further family studies and clinical correlation recommended.

⚠️ When to Consult a Doctor:

If you have symptoms of recurrent infections, fever, fatigue, or a family history of neutrophilia, consult a hematologist or geneticist for evaluation.

Limitations

  • ⚠May not detect all types of mutations
  • ⚠Requires interpretation by a geneticist
  • ⚠Not a diagnostic test for leukemia alone

Risks & Considerations

  • ●Minimal risk from blood draw: bruising, infection
  • ●Psychological impact of genetic results
  • ●Privacy concerns with genetic data

Interfering Factors

  • ●Sample contamination
  • ●Degraded DNA
  • ●Recent blood transfusion

Compare With Similar Tests

TestCSF3R Gene Neutrophilia, hereditary NGS Genetic TestJAK2 Mutation TestWhole Exome SequencingComplete Blood Count (CBC)
ComparisonCSF3R Gene Neutrophilia, hereditary NGS Genetic TestFor myeloproliferative disorders, not specific to neutrophilia.Broader genetic analysis but more expensive and time-consuming.Initial screening for neutrophilia but not genetic confirmation.

Frequently Asked Questions

What is CSF3R Gene Neutrophilia?
CSF3R Gene Neutrophilia is a rare genetic disorder caused by mutations in the CSF3R gene, leading to increased production of neutrophils, a type of white blood cell, and associated health risks.
What are the symptoms of CSF3R Gene Neutrophilia?
Symptoms include recurrent infections, fever, fatigue, enlarged spleen, and an increased risk of developing blood cancers like leukemia.
How is CSF3R Gene Neutrophilia diagnosed?
Diagnosis is confirmed through genetic testing using next-generation sequencing (NGS) to detect mutations in the CSF3R gene.
What is the cost of the CSF3R Gene Neutrophilia test in India?
The cost at DNA Labs India is INR 20,000, which includes home sample collection across India.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities across India.
How long does it take to get the test results?
Results are typically available within 3 to 4 weeks after sample collection.
What does a positive test result mean?
A positive result indicates the presence of a pathogenic variant in the CSF3R gene, confirming hereditary neutrophilia and increasing the risk for blood cancers.
Can this test detect all mutations in the CSF3R gene?
The test uses NGS to screen for known mutations, but it may not detect all possible variants. Genetic counseling is recommended for interpretation.
Is genetic counseling required before the test?
Yes, genetic counseling is recommended to understand the test implications, family risks, and to draw a pedigree chart.
What are the risks of the test?
The test involves minimal risks from blood draw, such as bruising. There may be psychological impacts from results, and genetic privacy should be considered.
How accurate is the NGS genetic test?
NGS is a highly accurate method for detecting genetic mutations, with high sensitivity and specificity for known variants.
What should I do if I have a family history of neutrophilia?
Consult a healthcare provider or geneticist for evaluation and consider genetic testing to confirm diagnosis and assess risks.
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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For Hospitals & Clinics

Reference Laboratory Services

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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