ATXN8OS Gene Spinocerebellar ataxia type 8, autosomal dominant NGS Genetic Test
Short Name: SCA8 NGS Genetic Test
Also known as: Spinocerebellar Ataxia Type 8, SCA8, ATXN8OS-related Ataxia
ATXN8OS Gene Spinocerebellar ataxia type 8, autosomal dominant NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS (Next-Generation Sequencing) 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 Pasupathy Arumugam
Consultant Pathologist · Reg: 21521
Last reviewed: September 7, 2026
Overview
To diagnose Spinocerebellar Ataxia Type 8 by detecting mutations in the ATXN8OS gene using NGS technology, aiding in clinical management and genetic counseling.
- Test Code
- 4581
- 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 (Next-Generation Sequencing)
Sample Collection
No special preparation required. Provide clinical history and genetic counseling session.
Laboratory Analysis
Blood sample will be drawn by a trained phlebotomist using sterile equipment.
Report Delivery
Apply pressure to the puncture site to stop bleeding and avoid strenuous activity.
Timeline: 3 to 4 weeks
Patient Instructions
About This Test
Who Should Get This Test
To diagnose Spinocerebellar Ataxia Type 8 by detecting mutations in the ATXN8OS gene using NGS technology, aiding in clinical management and genetic counseling.
How to Prepare
- Ensure proper patient identification
- Use sterile collection tubes
- Label samples correctly
Doctor's Notes
Reviewed by Dr Pasupathy Arumugam — MBBS, MD (Pathology) · Reg. No. 21521
"Genetic testing for SCA8 is crucial for early diagnosis and family planning. Consult a genetic counselor for personalized advice."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Understanding Your Results
Positive
Mutation detected, consistent with SCA8 diagnosis. Genetic counseling recommended.
Negative
No mutation detected, SCA8 unlikely. Consider other causes if symptoms persist.
If you experience symptoms of ataxia or have a family history of SCA8, consult a neurologist or geneticist for evaluation and testing.
Risks & Considerations
- ●Minor bruising at puncture site
- ●Rare infection risk
- ●Fainting or dizziness during blood draw
Frequently Asked Questions
What is the ATXN8OS Gene Spinocerebellar Ataxia Type 8 NGS Genetic Test?
Why is this test recommended?
How is the test performed?
What is the cost of the test?
Is home sample collection available?
How long does it take to get results?
What do the results mean?
Are there any risks associated with the test?
Can this test be used for prenatal diagnosis?
What is the inheritance pattern of SCA8?
How accurate is the NGS method?
What should I do if the test is positive?
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.