CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic Test
Short Name: CSRP3 Cardiomyopathy NGS Test
Also known as: CSRP3 Gene Mutation Test, Hypertrophic Cardiomyopathy Type 12 Genetic Test, CSRP3 Cardiac Genetic Test
CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 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.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of the CSRP3 Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the CSRP3 gene associated with familial hypertrophic cardiomyopathy type 12. This aids in accurate diagnosis, risk assessment, personalized treatment planning, and genetic counseling for patients and their families.
- Test Code
- 2528
- 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
Sample Collection
Provide clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of family members affected with cardiomyopathy.
Method: Venipuncture for blood; FTA card for drop blood
Laboratory Analysis
A blood sample is drawn via venipuncture, or a saliva sample or one drop of blood on an FTA card is collected by a trained phlebotomist.
Report Delivery
Apply pressure to the puncture site to prevent bruising. Store the sample as per instructions before transport to the laboratory.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the CSRP3 Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the CSRP3 gene associated with familial hypertrophic cardiomyopathy type 12. This aids in accurate diagnosis, risk assessment, personalized treatment planning, and genetic counseling for patients and their families.
How to Prepare
- Fast for 4-6 hours if specified, though not typically required
- Bring identification and doctor's prescription
- Inform about any medications or health conditions
- Ensure sample is labeled correctly
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Early genetic testing for CSRP3 mutations is crucial for timely diagnosis and management of familial hypertrophic cardiomyopathy, helping to prevent complications and guide family screening."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted blood sample
- Insufficient sample volume
- Improper labeling or documentation
- Contaminated sample
Understanding Your Results
Positive (pathogenic variant detected)
Confirms diagnosis of CSRP3 gene cardiomyopathy; recommend cardiac evaluation, family screening, and genetic counseling.
Negative (no pathogenic variant detected)
No mutation found in CSRP3 gene; does not rule out other genetic causes; clinical correlation advised.
Variant of uncertain significance (VUS)
Genetic variant identified but clinical significance unclear; further testing and monitoring may be needed.
Consult a doctor if you experience symptoms like chest pain, shortness of breath, fainting, or have a family history of cardiomyopathy. After testing, discuss results with a genetic specialist or cardiologist for appropriate management.
Limitations
- ⚠May not detect all genetic variants or mutations in non-coding regions
- ⚠Results require interpretation in clinical context by a genetic specialist
- ⚠Does not replace comprehensive cardiac evaluation
Risks & Considerations
- ●Minimal risks from blood draw: bruising, soreness, or rare infection
- ●Psychological impact of genetic results; counseling recommended
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
- ●Improper sample handling or storage
Compare With Similar Tests
| Test | CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic Test | MYH7 Gene Cardiomyopathy NGS Test | MYBPC3 Gene Cardiomyopathy NGS Test | TNNT2 Gene Cardiomyopathy NGS Test | Cardiac Biomarker Panel |
|---|---|---|---|---|---|
| Comparison | CSRP3 Gene Cardiomyopathy, familial hypertrophic type 12 NGS Genetic Test |
Frequently Asked Questions
What is CSRP3 gene cardiomyopathy?
How is the NGS genetic test performed?
What is the cost of the CSRP3 gene cardiomyopathy NGS test in India?
How long does it take to get the test results?
Is home sample collection available for this test?
What are the symptoms of CSRP3 gene cardiomyopathy?
How accurate is the NGS genetic test for detecting CSRP3 mutations?
What if the test result is positive?
Is genetic counseling required before the test?
Can children undergo this genetic test?
Is the test covered by insurance schemes like PMJAY or CGHS?
What should I do after receiving the test results?
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₹20,000Reference Laboratory Services
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