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SYNE1 Gene Spinocerebellar ataxia type 8, autosomal recessive NGS Genetic Test

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SYNE1 Gene Spinocerebellar ataxia type 8, autosomal recessive NGS Genetic Test

Also known as: Spinocerebellar ataxia type 8, SCA8

SYNE1 Gene Spinocerebellar ataxia type 8, autosomal recessive NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses NGS Technology 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.

NGS Genetic TestAdults🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr Pasupathy Arumugam

Dr Pasupathy Arumugam

Consultant Pathologist · Reg: 21521

Last reviewed: September 7, 2026

Overview

To diagnose Spinocerebellar ataxia type 8 by detecting mutations in the SYNE1 gene using Next-Generation Sequencing.

Test Code
4578
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 Technology
Step 1

Sample Collection

Genetic counseling recommended. Provide clinical history and family pedigree.

Step 2

Laboratory Analysis

Your sample is analyzed using NGS Technology in our laboratory.

Step 3

Report Delivery

A certified pathologist reviews and signs your report. You receive it as a secure PDF via email and WhatsApp.

Timeline: 3 to 4 Weeks

Patient Instructions

1
Before the Test:Genetic counseling and clinical history assessment.

About This Test

Who Should Get This Test

To diagnose Spinocerebellar ataxia type 8 by detecting mutations in the SYNE1 gene using Next-Generation Sequencing.

How to Prepare

  • Collect blood sample in appropriate container.
  • For FTA card, use one drop of blood.

Doctor's Notes

Reviewed by — MBBS, MD (Pathology) · Reg. No. 21521

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card

Understanding Your Results

Results indicate the presence or absence of mutations in the SYNE1 gene associated with SCA8.
Mutation detected: Consistent with SCA8 diagnosis; clinical correlation and genetic counseling advised.
No mutation detected: SCA8 unlikely, but further clinical evaluation may be needed if symptoms persist.
Variant of uncertain significance: May require additional testing or family studies for clarification.
⚠️ When to Consult a Doctor:

If symptoms of ataxia or family history of SCA8 are present, consult a neurologist or geneticist for evaluation and testing.

Risks & Considerations

  • ●Emotional or psychological implications of test results.
  • ●Potential for incidental findings unrelated to SCA8.

Frequently Asked Questions

What is SYNE1 Gene Spinocerebellar ataxia type 8?
Spinocerebellar ataxia type 8 (SCA8) is a neurodegenerative disorder caused by mutations in the SYNE1 gene, affecting movement coordination and balance.
What are the common symptoms of SCA8?
Symptoms include difficulty with coordination, fine motor skills, speech, eye movements, and cognitive problems, typically starting in adulthood.
How is SCA8 diagnosed?
Diagnosis is through genetic testing, specifically NGS analysis of the SYNE1 gene to detect mutations.
What does the NGS genetic test involve?
Next-Generation Sequencing (NGS) technology sequences the entire SYNE1 gene quickly and accurately from a DNA sample.
What is the cost of the SYNE1 Gene SCA8 test at DNA Labs India?
The test costs INR 20,000, with free home sample collection available across India.
Is home sample collection available for this test?
Yes, DNA Labs India offers free home sample collection for online bookings in numerous cities.
How long does it take to receive the test results?
Results are typically delivered within 3 to 4 weeks via online portal, email, or WhatsApp.
What does a positive test result indicate?
A positive result confirms the presence of SYNE1 gene mutations associated with SCA8, aiding in diagnosis.
What does a negative test result mean?
A negative result suggests no pathogenic mutations were detected, but clinical correlation is recommended if symptoms persist.
Is genetic counseling necessary before taking this test?
Yes, genetic counseling is recommended to understand the implications, risks, and benefits of testing.
Can this test be used for carrier screening?
Yes, it can identify carriers of SYNE1 mutations in families with a history of SCA8.
What are the limitations of genetic testing for SCA8?
Limitations may include variants of uncertain significance and the need for clinical interpretation alongside test results.
Worried about the process? Our certified phlebotomists collect thousands of samples every month across India. The process takes under 5 minutes and is virtually painless. Questions? Message us on WhatsApp — we're here 7 days a week.

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For Hospitals & Clinics

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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.

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