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SNTA1 Gene Long QT syndrome type 12 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

SNTA1 Gene Long QT syndrome type 12 NGS Genetic Test

Also known as: LQTS Type 12 Genetic Test, SNTA1 Mutation Analysis, Long QT Syndrome Type 12 DNA Test

SNTA1 Gene Long QT syndrome type 12 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

The purpose of the SNTA1 Gene Long QT Syndrome Type 12 NGS Genetic Test is to identify mutations in the SNTA1 gene that cause LQTS Type 12. This helps in accurate diagnosis, risk assessment, family screening, and guiding treatment decisions to prevent life-threatening cardiac events.

Test Code
5265
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 affected family members are required before sample collection.

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:Provide clinical history and undergo genetic counseling. No fasting is required.
2
During the Test:A blood sample will be drawn from a vein in your arm or alternative samples as specified.
3
After the Test:Apply pressure to the collection site to prevent bleeding. Resume normal activities.

About This Test

Who Should Get This Test

The purpose of the SNTA1 Gene Long QT Syndrome Type 12 NGS Genetic Test is to identify mutations in the SNTA1 gene that cause LQTS Type 12. This helps in accurate diagnosis, risk assessment, family screening, and guiding treatment decisions to prevent life-threatening cardiac events.

How to Prepare

  • Blood sample should be collected in an EDTA tube.
  • Alternatively, extracted DNA or one drop of blood on an FTA card can be used.
  • Ensure proper labeling and transport to the lab.

Doctor's Notes

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

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

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

Understanding Your Results

Interpretation of the SNTA1 Gene NGS Genetic Test results involves identifying pathogenic mutations associated with LQTS Type 12. A positive result indicates a genetic cause for the condition, while a negative result may not entirely rule out LQTS if other genes are involved.
Positive Result: Pathogenic mutation detected in SNTA1 gene, confirming LQTS Type 12. Genetic counseling and cardiac evaluation are recommended.
Negative Result: No pathogenic variants found in SNTA1 gene. Consider testing for other LQTS genes if clinical suspicion remains.
Variant of Uncertain Significance (VUS): A genetic change with unknown clinical significance. Further testing and family studies may be needed.
⚠️ When to Consult a Doctor:

Consult a healthcare provider if you experience symptoms like fainting, irregular heartbeat, or chest pain, especially with a family history of LQTS. After testing, discuss results with a geneticist or cardiologist for management.

Limitations

  • This test only analyzes the SNTA1 gene; other LQTS-related genes are not covered.
  • Results may require confirmation with additional clinical evaluation.
  • Genetic variants of uncertain significance may be identified.

Risks & Considerations

  • Minor pain or bruising at the blood draw site
  • Rare risk of infection or fainting during collection

Frequently Asked Questions

What is SNTA1 Gene Long QT Syndrome Type 12?
LQTS Type 12 is a heart condition caused by mutations in the SNTA1 gene, leading to irregular heartbeats and risk of sudden cardiac arrest.
What are the symptoms of LQTS Type 12?
Symptoms include fainting, irregular heartbeat, rapid heartbeat, shortness of breath, and chest pain, often during exercise or stress.
How is LQTS Type 12 diagnosed?
Diagnosis is through genetic testing using NGS technology to detect SNTA1 gene mutations, often supplemented with ECGs.
What is the cost of the SNTA1 Gene NGS Genetic Test?
The test costs INR 20000, with home sample collection available across India.
Is home sample collection available for this test?
Yes, free home sample collection is offered for online bookings in numerous cities across India.
How long does it take to get the test results?
Results are typically available in 3 to 4 weeks after sample collection.
What sample is required for the test?
The test requires blood, extracted DNA, or one drop of blood on an FTA card.
Is fasting required for this test?
No, fasting is not required for the SNTA1 Gene NGS Genetic Test.
Can this test be done for children?
Yes, the test can be performed on individuals of all ages, including children, with appropriate consent.
What if a mutation is found in the SNTA1 gene?
A positive result confirms LQTS Type 12. Genetic counseling and cardiac evaluation are recommended for management and family screening.
Is genetic counseling recommended before testing?
Yes, a genetic counseling session is advised to understand the test, draw a family pedigree, and discuss implications.
How accurate is the NGS technology for this test?
NGS technology provides high accuracy for detecting mutations in the SNTA1 gene, but results should be interpreted in clinical context.
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 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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