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CLCNKB Gene Bartter syndrome type 3 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

CLCNKB Gene Bartter syndrome type 3 NGS Genetic Test

Also known as: CLCNKB Gene Mutation Test, Bartter Syndrome Type 3 Genetic Test

CLCNKB Gene Bartter syndrome type 3 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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.

NGS Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To diagnose Bartter syndrome type 3 by detecting mutations in the CLCNKB gene using NGS technology.

Test Code
2562
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
NGS Technology
Step 1

Sample Collection

Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Bartter syndrome type 3.

Step 2

Laboratory Analysis

Your sample is analyzed using NGS Technology in our laboratory.

Step 3

Report Delivery

A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with Bartter syndrome type 3.

About This Test

Who Should Get This Test

To diagnose Bartter syndrome type 3 by detecting mutations in the CLCNKB gene using NGS technology.

How to Prepare

  • Blood sample collection by venipuncture
  • FTA card collection for one drop blood

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

"This test is crucial for diagnosing Bartter syndrome type 3, especially in patients with symptoms of electrolyte imbalances and kidney dysfunction."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card

Understanding Your Results

Results indicate the presence or absence of mutations in the CLCNKB gene associated with Bartter syndrome type 3.
📊

Pathogenic variant detected

Diagnosis of Bartter syndrome type 3 confirmed

📊

No pathogenic variant detected

Bartter syndrome type 3 unlikely, but clinical correlation needed

⚠️ When to Consult a Doctor:

If experiencing symptoms like excessive urination, thirst, or electrolyte imbalances, consult a nephrologist or geneticist.

Risks & Considerations

  • Minor bruising at blood draw site
  • Infection risk (very low)

Frequently Asked Questions

What is the CLCNKB Gene Bartter Syndrome Type 3 NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to detect mutations in the CLCNKB gene, which causes Bartter syndrome type 3.
Who should take this test?
Individuals with symptoms of Bartter syndrome type 3, such as excessive urination, thirst, electrolyte imbalances, or a family history of the disorder.
What are the symptoms of Bartter syndrome type 3?
Symptoms include polyuria, polydipsia, dehydration, hypokalemia, hypocalcemia, hypomagnesemia, and growth delays.
How is the test performed?
A blood sample or extracted DNA is collected and analyzed using NGS technology to identify mutations in the CLCNKB gene.
What is the cost of the test?
The test costs INR 20000.0 at DNA Labs India.
Is home sample collection available?
Yes, free home sample collection is available for online bookings across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What does a positive result mean?
A positive result indicates the presence of pathogenic mutations in the CLCNKB gene, confirming Bartter syndrome type 3.
What does a negative result mean?
A negative result means no pathogenic variants were detected, making Bartter syndrome type 3 unlikely, but clinical correlation is advised.
Are there any risks associated with the test?
Risks are minimal and include minor bruising at the blood draw site and a very low infection risk.
Is genetic counseling required?
Yes, a genetic counseling session is recommended before testing to draw a pedigree chart of affected family members.
How accurate is the test?
The test has a sensitivity of over 99% for detecting mutations in the CLCNKB gene.
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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Your Data Privacy

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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