KCNE2 Gene Long QT syndrome type 6 NGS Genetic Test
Short Name: KCNE2 LQTS Type 6 NGS Test
Also known as: LQTS Type 6, KCNE2-related Long QT Syndrome, Cardiac Channelopathy
KCNE2 Gene Long QT syndrome type 6 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.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
To identify pathogenic variants in the KCNE2 gene associated with Long QT Syndrome Type 6 for accurate diagnosis and risk assessment.
- Test Code
- 2533
- 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)
Sample Collection
Genetic counseling session and clinical history review.
Method: Venipuncture or finger prick
Laboratory Analysis
Blood sample drawn from vein or finger prick.
Report Delivery
Sample labeled and transported to laboratory.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify pathogenic variants in the KCNE2 gene associated with Long QT Syndrome Type 6 for accurate diagnosis and risk assessment.
How to Prepare
- Ensure proper identification
- Follow any specific instructions from healthcare provider
- Avoid strenuous activity before sample collection
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for KCNE2 mutations is essential for identifying individuals at risk of Long QT Syndrome Type 6, enabling preventive measures and personalized treatment."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted sample
- Insufficient sample volume
- Incorrect labeling
Understanding Your Results
Positive
Pathogenic variant detected, indicating increased risk for LQTS Type 6. Clinical correlation and genetic counseling recommended.
Negative
No pathogenic variant detected. However, clinical symptoms may require further evaluation.
Variant of Uncertain Significance
Genetic variant found but significance unknown. Further testing and family studies may be needed.
If you experience symptoms like fainting, palpitations, or have a family history of sudden cardiac death.
Limitations
- ⚠May not detect all genetic variants
- ⚠Requires interpretation by a geneticist
- ⚠Not a standalone diagnostic tool
Risks & Considerations
- ●Minimal risk from blood draw (bruising, infection)
- ●Psychological impact of genetic results
- ●Privacy concerns with genetic data
Interfering Factors
- ●Sample contamination
- ●Improper sample storage
- ●Recent blood transfusion
Compare With Similar Tests
| Test | KCNE2 Gene Long QT syndrome type 6 NGS Genetic Test | KCNQ1 Gene Long QT Syndrome Type 1 NGS Test | SCN5A Gene Long QT Syndrome Type 3 NGS Test | Comprehensive Cardiac Genetic Panel | ECG Test |
|---|---|---|---|---|---|
| Comparison | KCNE2 Gene Long QT syndrome type 6 NGS Genetic Test | Tests for a different gene associated with LQTS. | Focuses on sodium channel mutations. | Analyzes multiple genes for various cardiac disorders. | Non-genetic test for measuring QT interval. |
Frequently Asked Questions
What is the KCNE2 Gene Long QT Syndrome Type 6 NGS Genetic Test?
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What sample is required for the test?
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What are the symptoms of KCNE2 Gene Long QT Syndrome Type 6?
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Is genetic counseling provided with the test?
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₹20,000Reference 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.
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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