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SLC12A7 Gene Bartter syndrome NGS Genetic Test

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SLC12A7 Gene Bartter syndrome NGS Genetic Test

Short Name: SLC12A7 Bartter Syndrome NGS Test

Also known as: Bartter Syndrome Genetic Test, SLC12A7 Mutation Analysis

SLC12A7 Gene Bartter syndrome 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 confirm the diagnosis of Bartter syndrome by identifying mutations in the SLC12A7 gene and other related genes, enabling personalized treatment and management.

Test Code
2563
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 counselling session to draw a pedigree chart of family members affected with Bartter syndrome.

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:Genetic counselling and clinical history review.
2
During the Test:Sample collection and NGS analysis.
3
After the Test:Report generation and consultation with healthcare provider.

About This Test

Who Should Get This Test

To confirm the diagnosis of Bartter syndrome by identifying mutations in the SLC12A7 gene and other related genes, enabling personalized treatment and management.

How to Prepare

  • Provide clinical history
  • Attend genetic counselling session
  • Sample collection via blood draw or FTA card

Doctor's Notes

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

"This test is essential for confirming Bartter syndrome diagnosis and guiding personalized treatment plans to manage symptoms and prevent kidney damage."

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 SLC12A7 gene and other Bartter syndrome-related genes.
Positive result: Mutation detected, confirming Bartter syndrome.
Negative result: No mutation detected, but clinical correlation is needed.
Variant of uncertain significance: Further testing or family studies may be required.
⚠️ When to Consult a Doctor:

If experiencing symptoms of Bartter syndrome such as muscle weakness, fatigue, or excessive thirst, or if there is a family history of the disorder.

Risks & Considerations

  • Minimal risks associated with blood draw
  • No significant genetic test risks

Frequently Asked Questions

What is Bartter syndrome?
Bartter syndrome is a rare genetic disorder affecting the kidneys, causing electrolyte imbalances and symptoms like muscle weakness and fatigue.
What is the SLC12A7 gene?
The SLC12A7 gene provides instructions for making the Na-K-2Cl cotransporter protein, involved in kidney salt and water transport.
How is the SLC12A7 Gene Bartter Syndrome NGS Genetic Test performed?
It uses next-generation sequencing (NGS) to analyze the SLC12A7 gene and other related genes from a blood or DNA sample.
What is the cost of the test?
The test costs INR 20,000 at DNA Labs India, with home sample collection available.
Is home sample collection available?
Yes, free home sample collection is offered for online bookings across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks.
What are the symptoms of Bartter syndrome?
Symptoms include muscle weakness, fatigue, excessive thirst, dehydration, abdominal pain, constipation, and kidney damage.
Who should get this test?
Individuals with symptoms of Bartter syndrome or a family history of the disorder should consider this test.
Is the test covered by insurance?
Coverage depends on the insurance provider; check with your insurer for details.
What is NGS technology?
Next-generation sequencing (NGS) is an advanced genetic testing method that sequences DNA to identify mutations accurately.
Can this test be done for children?
Yes, the test is suitable for all ages, but genetic counselling is recommended.
What should I do after getting the test results?
Consult with a healthcare provider or genetic counsellor to interpret results and discuss treatment options.
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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LIMS Integration

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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