RYR2 Gene Arrhythmogenic right ventricular dysplasia type 2 NGS Genetic Test
Short Name: RYR2 ARVD2 NGS Test
Also known as: ARVD2, Arrhythmogenic Right Ventricular Dysplasia Type 2, RYR2-related ARVD
RYR2 Gene Arrhythmogenic right ventricular dysplasia type 2 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
To identify mutations in the RYR2 gene associated with Arrhythmogenic Right Ventricular Dysplasia Type 2 (ARVD2) for diagnostic confirmation, risk assessment, and family screening.
- Test Code
- 2485
- 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
Clinical history of the patient and a genetic counseling session to draw a pedigree chart of family members affected with ARVD2.
Method: Venipuncture
Laboratory Analysis
Standard blood draw procedure using aseptic technique.
Report Delivery
Apply pressure to the puncture site to prevent bleeding. Keep the area clean.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
To identify mutations in the RYR2 gene associated with Arrhythmogenic Right Ventricular Dysplasia Type 2 (ARVD2) for diagnostic confirmation, risk assessment, and family screening.
How to Prepare
- Fast for 8-12 hours if specified, but not required for this test.
- Bring identification and doctor's prescription.
- Inform about any medications or health conditions.
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for RYR2 gene mutations is essential for confirming ARVD2 diagnosis and guiding treatment plans to prevent life-threatening arrhythmias."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed samples
- Insufficient sample volume
- Improperly labeled samples
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of ARVD2. Recommend clinical evaluation and family screening.
No pathogenic variant detected
ARVD2 unlikely, but clinical correlation is advised. Consider other genetic or non-genetic causes.
Variant of uncertain significance
Further testing and family studies may be needed. Consult a genetic counselor.
If you experience symptoms like chest pain, palpitations, or fainting, or have a family history of ARVD2 or sudden cardiac death, consult a cardiologist or genetic specialist.
Limitations
- ⚠May not detect all types of mutations
- ⚠Requires genetic counseling for interpretation
- ⚠Results may have variants of uncertain significance
Risks & Considerations
- ●Minimal risk from blood draw: bruising, infection
- ●Psychological impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
Compare With Similar Tests
| Test | RYR2 Gene Arrhythmogenic right ventricular dysplasia type 2 NGS Genetic Test | Sanger Sequencing | ECG | Cardiac MRI |
|---|---|---|---|---|
| Comparison | RYR2 Gene Arrhythmogenic right ventricular dysplasia type 2 NGS Genetic Test |
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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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