MYL3 Gene Cardiomyopathy, familial hypertrophic type 8 NGS Genetic Test
Short Name: MYL3 Gene Cardiomyopathy NGS Test
Also known as: MYL3 Gene Test, HCM Type 8 Genetic Test, Familial Hypertrophic Cardiomyopathy Genetic Test
MYL3 Gene Cardiomyopathy, familial hypertrophic type 8 NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) 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 MYL3 Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the MYL3 gene that cause familial hypertrophic cardiomyopathy type 8. This helps in confirming diagnosis, assessing risk for family members, guiding personalized treatment plans, and facilitating genetic counseling.
- Test Code
- 5235
- 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
- Next-Generation Sequencing (NGS)
Sample Collection
Provide clinical history of the patient and undergo a genetic counseling session to draw a pedigree chart of affected family members.
Method: Venipuncture or Blood drop on FTA Card
Laboratory Analysis
A blood sample will be collected via venipuncture or a blood drop on an FTA card by a trained phlebotomist.
Report Delivery
Apply pressure to the puncture site to prevent bruising. The sample will be processed and sent for NGS analysis.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the MYL3 Gene Cardiomyopathy NGS Genetic Test is to identify mutations in the MYL3 gene that cause familial hypertrophic cardiomyopathy type 8. This helps in confirming diagnosis, assessing risk for family members, guiding personalized treatment plans, and facilitating genetic counseling.
How to Prepare
- Ensure proper patient identification and sample labeling
- Avoid hemolysis by gentle mixing of blood samples
- Store samples at room temperature if using FTA cards, or refrigerate blood tubes
- Transport samples to the lab within 48 hours
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for MYL3 mutations is crucial for early diagnosis and management of familial hypertrophic cardiomyopathy, helping to guide treatment and family screening."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Improperly labeled or contaminated samples
- Samples older than stability period
Understanding Your Results
Positive for pathogenic variant
Confirms diagnosis of familial hypertrophic cardiomyopathy type 8 due to MYL3 mutation. Genetic counseling and family screening recommended.
Negative for pathogenic variant
No MYL3 mutations detected. Clinical correlation and further testing may be needed if symptoms persist.
Variant of uncertain significance (VUS)
A genetic variant was found, but its clinical significance is unknown. Repeat testing or family studies may be advised.
Consult a doctor if you experience symptoms like chest pain, shortness of breath, or fainting, or if you have a family history of cardiomyopathy. Genetic counseling is recommended before and after testing.
Limitations
- ⚠May not detect all types of genetic variants, such as large deletions or duplications
- ⚠Results require interpretation by a genetic counselor or specialist
- ⚠Genetic testing cannot predict disease severity or onset in all cases
Risks & Considerations
- ●Minor bruising or discomfort at the blood draw site
- ●Rare risk of infection or hematoma
- ●Emotional impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA quality
- ●Hemolyzed or clotted blood samples
- ●Incorrect sample storage or handling
Compare With Similar Tests
| Test | MYL3 Gene Cardiomyopathy, familial hypertrophic type 8 NGS Genetic Test | MYH7 Gene Cardiomyopathy Test | TNNT2 Gene Cardiomyopathy Test | Comprehensive Cardiomyopathy Panel |
|---|---|---|---|---|
| Comparison | MYL3 Gene Cardiomyopathy, familial hypertrophic type 8 NGS Genetic Test |
Frequently Asked Questions
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