ACTC1 Gene Cardiomyopathy, dilated type 1R NGS Genetic Test
Short Name: ACTC1 DCM 1R Test
Also known as: ACTC1-related cardiomyopathy, DCM Type 1R, Alpha-cardiac actin cardiomyopathy
ACTC1 Gene Cardiomyopathy, dilated type 1R NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS), Genetic Sequencing on Blood samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To diagnose mutations in the ACTC1 gene that cause dilated cardiomyopathy type 1R, enabling early intervention, family screening, and personalized treatment plans.
- Test Code
- 5221
- Price
- ₹20,000
- Sample Type
- Blood
- Result Time
- 3 to 4 Weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS), Genetic Sequencing
Sample Collection
No specific preparation required. Provide clinical history and family pedigree during genetic counseling.
Method: Venipuncture
Laboratory Analysis
A blood sample is drawn from a vein in the arm using standard venipuncture techniques.
Report Delivery
Apply pressure to the puncture site to prevent bleeding. Resume normal activities unless advised otherwise.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose mutations in the ACTC1 gene that cause dilated cardiomyopathy type 1R, enabling early intervention, family screening, and personalized treatment plans.
How to Prepare
- Ensure proper identification of the patient
- Use sterile equipment for blood collection
- Label the sample correctly with patient details
- Transport the sample to the lab within the specified stability period
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Genetic testing for ACTC1 mutations is crucial for early diagnosis, family screening, and personalized management of dilated cardiomyopathy."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Incorrect labeling or missing patient information
Understanding Your Results
Positive for pathogenic variant
Confirms diagnosis; recommend genetic counseling and family screening
Negative for pathogenic variant
No mutation detected; clinical correlation needed if symptoms persist
Variant of uncertain significance
Further testing and monitoring may be required
Consult a cardiologist or geneticist immediately if you experience symptoms like shortness of breath, chest pain, or if you have a family history of heart disease. After testing, discuss results with a healthcare provider for appropriate management.
Limitations
- ⚠May not detect all genetic variants or mutations
- ⚠Results require interpretation by a genetic counselor or specialist
- ⚠Does not replace clinical evaluation and other diagnostic tests
Risks & Considerations
- ●Minimal risks from blood draw, such as bruising or infection
- ●Psychological impact of genetic results, including anxiety
- ●Potential for incidental findings unrelated to cardiomyopathy
Interfering Factors
- ●Poor sample quality or contamination
- ●Recent blood transfusions may affect DNA analysis
- ●Inadequate sample volume or improper storage
Compare With Similar Tests
| Test | ACTC1 Gene Cardiomyopathy, dilated type 1R NGS Genetic Test | TTN Gene Cardiomyopathy Test | LMNA Gene Cardiomyopathy Test | MYH7 Gene Cardiomyopathy Test | Cardiac MRI |
|---|---|---|---|---|---|
| Comparison | ACTC1 Gene Cardiomyopathy, dilated type 1R NGS Genetic Test |
Frequently Asked Questions
What is ACTC1 gene cardiomyopathy, dilated type 1R?
How is the ACTC1 gene test performed?
What is the cost of the ACTC1 gene test in India?
Is home sample collection available for this test?
How long does it take to get the test results?
What do positive test results mean?
Is genetic counseling required before testing?
Can this test be used for family screening?
What are the risks of the genetic test?
Is the test covered by insurance schemes like PMJAY?
How accurate is the NGS genetic test for ACTC1?
What should I do if I test positive for an ACTC1 mutation?
Related Tests
Angelman Syndrome Test
₹10,000Duchenne / Becker Muscular Dystrophy (DMD / BMD) Gene Mutation Test
₹14,000Episodic Ataxia Type 1 Hotspot Test
₹11,500Episodic Ataxia Comprehensive Profile Hotspot Test
₹16,000Megalencephalic Leukoencephalopathy with Subcortical Cysts Van Der Knaap and Nalband MLC Gene Hotspot Mutation Test
₹7,500Analyzer 18 SMA 18 Test Panel
₹1,755Reference 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.
Book Your Test
Enter your details and we'll connect you within 15 minutes.
