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CALM1 Gene Ventricular tachycardia, catecholaminergic polymorphic type 4 NGS Genetic Test

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CALM1 Gene Ventricular tachycardia, catecholaminergic polymorphic type 4 NGS Genetic Test

Short Name: CALM1 Gene CPVT Type 4 NGS Test

Also known as: CALM1-related CPVT, CPVT type 4 genetic test, Calmodulin 1 gene test

CALM1 Gene Ventricular tachycardia, catecholaminergic polymorphic type 4 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 Results available in 3 to 4 weeks after sample receipt.. Free home collection in 300+ cities across India.

Genetic Test🏠 Home Collection

🩺 Medically Reviewed By

Overview

To detect mutations in the CALM1 gene that cause catecholaminergic polymorphic ventricular tachycardia type 4, facilitating diagnosis, risk stratification, and genetic counseling for patients and families.

Test Code
5304
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
Results available in 3 to 4 weeks after sample receipt.
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

No specific preparation required. Provide clinical history and family pedigree during genetic counseling.

Method: Venipuncture or blood drop

Step 2

Laboratory Analysis

Blood sample collected via venipuncture or blood drop on FTA card by trained phlebotomist.

Step 3

Report Delivery

Apply pressure to the puncture site to prevent bruising. Store sample as per instructions.

Timeline: Results available in 3 to 4 weeks after sample receipt.

Patient Instructions

1
Before the Test:Undergo genetic counseling to understand implications. Provide detailed medical and family history.
2
During the Test:Blood sample collection; procedure takes about 10-15 minutes.
3
After the Test:Resume normal activities. Await results in 3-4 weeks; follow up with healthcare provider.

About This Test

Who Should Get This Test

To detect mutations in the CALM1 gene that cause catecholaminergic polymorphic ventricular tachycardia type 4, facilitating diagnosis, risk stratification, and genetic counseling for patients and families.

How to Prepare

  • Ensure proper identification of patient
  • Use sterile equipment
  • Label samples correctly
  • Transport samples at recommended temperature

Doctor's Notes

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

"Genetic testing for CPVT type 4 via CALM1 gene analysis is crucial for accurate diagnosis, risk assessment, and guiding family screening to prevent 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 Volume5-10 ml blood
ContainerEDTA tube or FTA card
Collection MethodVenipuncture or blood drop

Sample Stability

Blood in EDTA tube: stable for 7 days at 2-8°C
FTA card: stable at room temperature for extended periods
Sample Rejection Criteria:
  • Hemolyzed or clotted samples
  • Incorrectly labeled samples
  • Insufficient sample volume
  • Contaminated samples

Understanding Your Results

Results indicate the presence or absence of pathogenic variants in the CALM1 gene. Positive results confirm genetic predisposition to CPVT type 4, while negative results may require further testing if clinical suspicion remains high.
📊

Pathogenic variant detected

Confirms diagnosis of CPVT type 4; recommend clinical management and family screening

📊

No pathogenic variant detected

Reduces likelihood of CALM1-related CPVT; consider other genetic or non-genetic causes

📊

Variant of uncertain significance (VUS)

Requires further evaluation and genetic counseling; may not be causative

⚠️ When to Consult a Doctor:

Consult a cardiologist or geneticist if you experience symptoms like fainting, palpitations, or have a family history of CPVT. After receiving test results, seek professional guidance for management and family screening.

Limitations

  • May not detect all genetic variants due to technical limitations
  • Variants of uncertain significance (VUS) may require further evaluation
  • Does not rule out other genetic or non-genetic causes of CPVT
  • Results should be correlated with clinical findings

Risks & Considerations

  • Minimal risk from blood draw: bruising, infection, or discomfort
  • Psychological impact of genetic results; counseling recommended

Interfering Factors

  • Poor sample quality or contamination
  • Recent blood transfusion
  • Inadequate sample volume
  • Technical errors in sequencing

Compare With Similar Tests

TestCALM1 Gene Ventricular tachycardia, catecholaminergic polymorphic type 4 NGS Genetic TestRYR2 Gene CPVT TestCASQ2 Gene CPVT TestTRDN Gene CPVT TestComprehensive CPVT Panel
ComparisonCALM1 Gene Ventricular tachycardia, catecholaminergic polymorphic type 4 NGS Genetic Test

Frequently Asked Questions

What is the CALM1 gene?
The CALM1 gene encodes calmodulin, a protein that regulates calcium signaling in cells, including heart muscle cells.
What is CPVT type 4?
CPVT type 4 is a genetic cardiac disorder caused by mutations in the CALM1 gene, leading to life-threatening arrhythmias triggered by stress or exercise.
Who should consider this genetic test?
Individuals with symptoms of CPVT, family history of sudden cardiac death, or unexplained cardiac events should consider testing.
How is the test performed?
The test uses next-generation sequencing (NGS) to analyze the CALM1 gene from a blood or DNA sample.
What does a positive result mean?
A positive result indicates a pathogenic variant in CALM1, confirming genetic predisposition to CPVT type 4, requiring clinical management.
What if the result is negative?
A negative result reduces the likelihood of CALM1-related CPVT, but other genetic or non-genetic causes may exist; consult your doctor.
Is genetic counseling required?
Yes, genetic counseling is recommended before and after testing to understand implications and guide decision-making.
What is the cost of the test?
The test costs INR 20000 at DNA Labs India, with home sample collection available across India.
How long does it take to get results?
Results are typically available in 3 to 4 weeks after sample collection.
Is the test covered by insurance?
Coverage varies; check with your insurance provider. DNA Labs India offers affordable pricing.
Can this test be done at home?
Yes, DNA Labs India provides free home sample collection for online bookings in many cities across India.
What are the risks of the test?
Risks are minimal, mainly related to blood draw, such as bruising. Psychological impact may occur; counseling is available.
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 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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