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KCNQ1 Gene Long QT syndrome type 1 NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

KCNQ1 Gene Long QT syndrome type 1 NGS Genetic Test

Short Name: KCNQ1 LQTS Type 1 NGS Test

Also known as: LQTS Type 1 Genetic Test, KCNQ1 Mutation Analysis, Long QT Syndrome Type 1 NGS Test

KCNQ1 Gene Long QT syndrome type 1 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.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the KCNQ1 Gene Long QT Syndrome Type 1 NGS Genetic Test is to detect mutations in the KCNQ1 gene associated with Long QT syndrome type 1. This helps in confirming diagnosis, guiding treatment, assessing familial risk, and enabling genetic counseling for affected individuals and their families.

Test Code
5263
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

No specific preparation is required. Inform the healthcare provider about any medications or recent medical procedures.

Method: Venipuncture or saliva collection

Step 2

Laboratory Analysis

A blood sample will be drawn from a vein in the arm, or a saliva sample may be collected. The process is quick and minimally invasive.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bleeding. Resume normal activities unless advised otherwise.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:No fasting required. Provide clinical history and undergo genetic counseling as recommended.
2
During the Test:Sample collection via blood draw or saliva. The test involves NGS analysis in the laboratory.
3
After the Test:Results are delivered in 3-4 weeks. Follow up with a healthcare provider for interpretation and next steps.

About This Test

Who Should Get This Test

The purpose of the KCNQ1 Gene Long QT Syndrome Type 1 NGS Genetic Test is to detect mutations in the KCNQ1 gene associated with Long QT syndrome type 1. This helps in confirming diagnosis, guiding treatment, assessing familial risk, and enabling genetic counseling for affected individuals and their families.

How to Prepare

  • Ensure proper identification and labeling of the sample
  • Use sterile collection equipment
  • Follow standard phlebotomy or saliva collection protocols
  • Transport sample to the lab within the specified stability period

Doctor's Notes

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

"Genetic testing for Long QT syndrome is crucial for early diagnosis, risk assessment, and management, especially in families with a history of sudden cardiac events."

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 blood or equivalent
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or saliva collection

Sample Stability

Blood sample: Stable for 48 hours at 2-8°C
Extracted DNA: Stable for years at -20°C
FTA card: Stable at room temperature for extended periods
Sample Rejection Criteria:
  • Hemolyzed or clotted blood samples
  • Insufficient sample volume
  • Improper labeling or documentation
  • Sample contamination

Understanding Your Results

Results from the KCNQ1 Gene Long QT Syndrome Type 1 NGS Genetic Test should be interpreted by a qualified geneticist or cardiologist. A positive result indicates the presence of a mutation in the KCNQ1 gene, confirming a diagnosis of LQTS type 1. A negative result does not entirely rule out LQTS, as other genes may be involved.
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Positive for pathogenic variant

Confirms diagnosis of Long QT syndrome type 1. Recommend clinical evaluation, family screening, and management strategies.

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Negative for pathogenic variant

No mutation detected in KCNQ1 gene. Consider other genetic causes or clinical assessment if symptoms persist.

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Variant of uncertain significance (VUS)

Further testing and family studies may be needed. Clinical correlation is essential.

⚠️ When to Consult a Doctor:

Consult a doctor if you experience symptoms like fainting, irregular heartbeat, or chest pain, especially with a family history of LQTS. After receiving test results, seek genetic counseling or cardiology consultation for management.

Limitations

  • May not detect all genetic variants or mutations in non-coding regions
  • Results require interpretation by a genetic specialist
  • Does not replace clinical evaluation or other cardiac tests
  • False negatives or positives are possible, though rare

Risks & Considerations

  • Minimal risks from blood draw, such as bruising or infection
  • Psychological impact of genetic results
  • Potential for inconclusive results requiring further testing

Interfering Factors

  • Sample contamination or degradation
  • Insufficient DNA quantity or quality
  • Recent blood transfusions may affect results
  • Technical errors in sequencing

Frequently Asked Questions

What is the KCNQ1 Gene Long QT Syndrome Type 1 NGS Genetic Test?
It is a genetic test that uses Next-Generation Sequencing to analyze the KCNQ1 gene for mutations causing Long QT syndrome type 1, an inherited heart condition.
Who should consider this test?
Individuals with a family history of LQTS, unexplained cardiac symptoms like fainting or irregular heartbeat, or those seeking genetic counseling.
What is the cost of the test in India?
The cost is approximately INR 20,000, which may vary slightly by location and includes home sample collection.
How is the test performed?
A blood or saliva sample is collected and analyzed using NGS technology to detect mutations in the KCNQ1 gene.
Is fasting required before the test?
No, fasting is not required for this genetic test.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the results mean?
A positive result confirms a mutation in the KCNQ1 gene, indicating LQTS type 1. A negative result means no mutation was detected, but clinical evaluation may still be needed.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for online bookings across many cities in India.
What are the risks of the test?
Risks are minimal, such as bruising from blood draw. There may be psychological impacts from genetic results, so genetic counseling is recommended.
Can this test be used for family screening?
Yes, it is valuable for screening family members at risk of LQTS type 1, especially after a positive result in an affected individual.
What should I do after receiving the results?
Consult a geneticist or cardiologist for interpretation, management options, and family planning advice.
Is the test covered by insurance?
Coverage depends on the insurance policy. It is not typically covered under government schemes like PMJAY, but check with your provider.
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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