ABCC9 Gene Cardiomyopathy, dilated type 1O NGS Genetic Test
Short Name: ABCC9 Cardiomyopathy NGS Test
Also known as: Dilated Cardiomyopathy Type 1O, ABCC9-related Cardiomyopathy
ABCC9 Gene Cardiomyopathy, dilated type 1O NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood 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
To identify mutations in the ABCC9 gene associated with dilated cardiomyopathy type 1O for diagnosis, genetic counseling, and management planning.
- Test Code
- 5220
- Price
- ₹20,000
- Sample Type
- Blood
- Result Time
- 3 to 4 weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
Clinical history review and genetic counseling session recommended to draw a pedigree chart of affected family members.
Method: Venipuncture
Laboratory Analysis
Blood sample collected via venipuncture by a trained phlebotomist.
Report Delivery
Sample is processed and sent to the laboratory for NGS analysis.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the ABCC9 gene associated with dilated cardiomyopathy type 1O for diagnosis, genetic counseling, and management planning.
How to Prepare
- Ensure proper patient identification
- Use sterile collection equipment
- Label samples correctly with patient details
- Follow standard blood collection protocols
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for ABCC9 gene cardiomyopathy is essential for accurate diagnosis and family planning. Early detection can lead to better management strategies."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted sample
- Incorrect labeling or insufficient volume
- Sample not stored properly
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of ABCC9 gene cardiomyopathy. Genetic counseling and cardiac management recommended.
No pathogenic variant detected
Reduces likelihood of ABCC9-related cardiomyopathy, but clinical correlation and further testing may be needed.
Variant of uncertain significance (VUS)
Further testing, family studies, and clinical follow-up are required for clarification.
If you experience symptoms like shortness of breath, fatigue, chest pain, or have a family history of cardiomyopathy, consult a cardiologist or geneticist immediately.
Limitations
- ⚠May not detect all possible mutations in the ABCC9 gene
- ⚠Variants of uncertain significance (VUS) may be reported
- ⚠Requires genetic counseling for accurate interpretation
- ⚠Does not rule out other causes of cardiomyopathy
Risks & Considerations
- ●Minimal risk from blood draw (e.g., bruising, infection)
- ●Potential for genetic discrimination concerns
- ●Psychological impact of results, requiring counseling
Interfering Factors
- ●Sample hemolysis
- ●Insufficient DNA quantity
- ●Contamination during collection or processing
Compare With Similar Tests
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Frequently Asked Questions
What is ABCC9 gene cardiomyopathy?
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₹20,000Reference 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.
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