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DNA Labs India

CSRP3 Gene Cardiomyopathy, dilated type 1M NGS Genetic Test

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CSRP3 Gene Cardiomyopathy, dilated type 1M NGS Genetic Test

Short Name: CSRP3 Gene Test

Also known as: CSRP3 Mutation Test, Dilated Cardiomyopathy 1M Genetic Test

CSRP3 Gene Cardiomyopathy, dilated type 1M 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

To detect mutations in the CSRP3 gene associated with dilated cardiomyopathy type 1M, aiding in diagnosis, risk assessment, and family genetic counseling.

Test Code
5217
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

Genetic counseling session to discuss family history and draw a pedigree chart. Provide clinical history of the patient.

Method: Venipuncture or FTA Card

Step 2

Laboratory Analysis

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

Step 3

Report Delivery

Sample processed for NGS analysis. Await results and schedule follow-up with physician.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical history assessment. No fasting required.
2
During the Test:Blood sample collection via venipuncture or FTA card.
3
After the Test:Wait for 3-4 weeks for results. Follow-up with physician for interpretation and next steps.

About This Test

Who Should Get This Test

To detect mutations in the CSRP3 gene associated with dilated cardiomyopathy type 1M, aiding in diagnosis, risk assessment, and family genetic counseling.

How to Prepare

  • Use sterile equipment for blood draw
  • Label samples correctly with patient details
  • Store FTA card at room temperature if used

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
Collection MethodVenipuncture or FTA Card

Sample Stability

Blood: 2-8°C for 7 days
FTA Card: Room temperature for years
Sample Rejection Criteria:
  • Hemolyzed sample
  • Incorrect labeling
  • Insufficient sample volume

Understanding Your Results

Results indicate the presence or absence of pathogenic mutations in the CSRP3 gene. Positive results confirm genetic predisposition to dilated cardiomyopathy type 1M.
Positive: Pathogenic variant detected – indicates genetic cause, recommend family screening and cardiology follow-up.
Negative: No pathogenic variant – does not rule out other genetic or non-genetic causes; clinical evaluation advised.
Variant of Uncertain Significance (VUS): Further research needed; genetic counseling recommended.
⚠️ When to Consult a Doctor:

If experiencing symptoms like shortness of breath, fatigue, or swelling, or if there is a family history of cardiomyopathy. After receiving test results, consult a cardiologist or genetic counselor for management.

Limitations

  • May not detect all genetic variants or non-CSRP3 related causes
  • Requires clinical correlation and genetic counseling
  • Results may have variants of uncertain significance

Risks & Considerations

  • Minor bruising at puncture site
  • Rare infection risk
  • Psychological impact of genetic results

Interfering Factors

  • Hemolyzed or degraded DNA sample
  • Insufficient sample volume
  • Contamination during collection

Frequently Asked Questions

What is the CSRP3 Gene Cardiomyopathy Dilated Type 1M NGS Genetic Test?
This test uses Next-Generation Sequencing to analyze the CSRP3 gene for mutations linked to dilated cardiomyopathy type 1M, a genetic heart condition.
Who should consider this genetic test?
Individuals with symptoms of dilated cardiomyopathy, family history of the condition, or those diagnosed with unexplained heart muscle disease.
What are the symptoms of CSRP3 gene cardiomyopathy?
Symptoms include shortness of breath, fatigue, swelling in legs/ankles/feet, irregular heartbeat, and chest pain, which may develop gradually.
How is the test performed?
A blood sample or DNA extract is collected and analyzed using NGS technology to detect mutations in the CSRP3 gene.
What is the cost of the test in India?
The test costs INR 20,000, with free home sample collection available across India.
Is genetic testing covered by insurance?
Genetic testing is not always covered by insurance. It's advisable to check with your insurance provider beforehand.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What does a positive result mean?
A positive result indicates a pathogenic mutation in the CSRP3 gene, confirming genetic predisposition to dilated cardiomyopathy. Genetic counseling is recommended.
Can this test be used for family screening?
Yes, genetic testing can identify at-risk family members, allowing for early monitoring and intervention.
Are there any risks associated with the test?
Risks are minimal, such as minor bruising from blood draw. Psychological impacts of results should be discussed with a counselor.
What should I do before the test?
Undergo genetic counseling to discuss family history and understand the test implications. No fasting is required.
How do I book the test?
Book online through DNA Labs India's website for home sample collection or visit a walk-in center. Contact for assistance.
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.

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