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DNA Labs India

Cardiac Channelopathy Gene Panel Test

DNA Labs India | ISO 9001:2015 Certified

Cardiac Channelopathy Gene Panel Test

Also known as: Cardiac Channelopathy Genetic Test, Channelopathy Gene Panel, Inherited Arrhythmia Gene Test

Cardiac Channelopathy Gene Panel Test test available at DNA Labs India for ₹36,000. Uses Next-Generation Sequencing (NGS) on Amniotic fluid/ Chorionic villi/ Peripheral blood samples. Results in 4-6 weeks. Free home collection in 300+ cities across India.

Genetic Panel🏠 Home Collection

🩺 Medically Reviewed By

Overview

The purpose of the Cardiac Channelopathy Gene Panel is to identify genetic mutations responsible for cardiac channelopathies, enabling accurate diagnosis, risk assessment, and personalized management. It aids in confirming clinical suspicions, guiding therapy such as medication or device implantation, and facilitating genetic counseling for affected families.

Test Code
2952
Price
₹36,000
Sample Type
Amniotic fluid/ Chorionic villi/ Peripheral blood
Result Time
4-6 weeks
Fasting Required
No
Method
Next-Generation Sequencing (NGS)
Step 1

Sample Collection

Ensure a doctor's prescription is available. For blood samples, no fasting is required. For prenatal samples, follow specific medical guidance.

Method: Venipuncture for blood; amniocentesis or chorionic villus sampling for prenatal samples

Step 2

Laboratory Analysis

Sample collection is performed by trained phlebotomists or medical professionals. For blood, a venipuncture is done; for amniotic fluid or chorionic villi, specialized procedures are required.

Step 3

Report Delivery

Apply pressure to the puncture site for blood samples. Store samples as per instructions and transport to the lab promptly.

Timeline: 4-6 weeks

Patient Instructions

1
Before the Test:Obtain a doctor's prescription. No special preparation is needed for blood samples. For prenatal testing, follow medical advice.
2
During the Test:Sample collection takes 10-15 minutes for blood; longer for prenatal procedures. Minimal discomfort expected.
3
After the Test:Resume normal activities. Results will be available online or via email/WhatsApp in 4-6 weeks.

About This Test

Who Should Get This Test

The purpose of the Cardiac Channelopathy Gene Panel is to identify genetic mutations responsible for cardiac channelopathies, enabling accurate diagnosis, risk assessment, and personalized management. It aids in confirming clinical suspicions, guiding therapy such as medication or device implantation, and facilitating genetic counseling for affected families.

How to Prepare

  • Use sterile containers for sample collection
  • Label samples correctly with patient details
  • Maintain sample integrity during transport
  • For prenatal samples, ensure proper medical supervision

Doctor's Notes

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

"This gene panel is crucial for diagnosing inherited cardiac channelopathies, which can lead to sudden cardiac events. Early detection allows for personalized management and family screening."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeAmniotic fluid/ Chorionic villi/ Peripheral blood
Sample VolumeVaries based on sample type
ContainerSterile container/ Sterile Normal Saline Container/ EDTA Vacutainer
Collection MethodVenipuncture for blood; amniocentesis or chorionic villus sampling for prenatal samples

Sample Stability

Peripheral blood: Stable for 48 hours at room temperature
Amniotic fluid: Stable for 24 hours refrigerated
Chorionic villi: Stable for 24 hours refrigerated
Sample Rejection Criteria:
  • Sample improperly labeled or contaminated
  • Insufficient sample volume
  • Sample not stored or transported correctly

Understanding Your Results

Test results indicate the presence or absence of genetic mutations associated with cardiac channelopathies. Positive results require clinical evaluation and genetic counseling.
Detected: Genetic mutation identified; correlate with clinical symptoms and family history
Not Detected: No mutations found in the tested genes; consider other diagnostic tests
Variant of Uncertain Significance (VUS): Further research and clinical follow-up needed
⚠️ When to Consult a Doctor:

Consult a cardiologist or geneticist immediately if test results are positive, or if symptoms persist despite negative results. Genetic counseling is recommended for family planning.

Limitations

  • May not detect all genetic variants or novel mutations
  • Results require clinical correlation and genetic counseling
  • Limited to genes included in the panel; does not cover all cardiac conditions

Risks & Considerations

  • For blood draw: Minor bruising, pain, or infection at puncture site
  • For prenatal samples: Risk of miscarriage or infection (rare)
  • Psychological impact of genetic results

Interfering Factors

  • Sample contamination during collection or transport
  • Degraded DNA due to improper storage
  • Presence of inhibitors in the sample affecting sequencing

Compare With Similar Tests

TestCardiac Channelopathy Gene PanelECG (Electrocardiogram)Cardiac MRILong QT Syndrome Gene Panel
ComparisonCardiac Channelopathy Gene Panel

Frequently Asked Questions

What is the Cardiac Channelopathy Gene Panel test?
It is a genetic test that analyzes multiple genes to identify mutations causing cardiac channelopathies, which are disorders of the heart's electrical system.
Who should take this test?
Individuals with a family history of cardiac channelopathies, unexplained fainting, arrhythmias, or symptoms like chest pain and shortness of breath.
How is the test performed?
The test uses next-generation sequencing (NGS) on DNA extracted from blood, amniotic fluid, or chorionic villi samples.
What samples are required for the test?
Peripheral blood, amniotic fluid, or chorionic villi samples collected in sterile containers.
What is the cost of the Cardiac Channelopathy Gene Panel test?
The cost is INR 36000 at DNA Labs India, with free home sample collection available across India.
How long does it take to receive the test results?
Results are typically available within 4-6 weeks after sample collection.
Is fasting required before the test?
No, fasting is not required for this test. It can be done with a doctor's prescription.
Are there any risks associated with the test?
Risks are minimal for blood draws, including minor bruising. For prenatal samples, there are rare risks like infection or miscarriage.
How accurate is the genetic test for cardiac channelopathies?
The test is highly accurate using NGS technology, but it may not detect all mutations. Results should be interpreted clinically.
What do the test results mean?
Results indicate if genetic mutations are detected. Positive results require consultation with a cardiologist or geneticist for management.
Is the test covered by health insurance schemes like PMJAY or CGHS?
Coverage varies; it is not typically covered under government schemes like PMJAY or CGHS. Check with your insurance provider.
Can I get the test done at home?
Yes, DNA Labs India offers free home sample collection for this test in many cities across India.
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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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.

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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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