Skip to main content
DNA Labs India

ATXN10 Gene Spinocerebellar ataxia type 10, autosomal dominant NGS Genetic Test

DNA Labs India | ISO 9001:2015 Certified

ATXN10 Gene Spinocerebellar ataxia type 10, autosomal dominant NGS Genetic Test

Short Name: ATXN10 Gene SCA10 Test

Also known as: Spinocerebellar ataxia type 10, SCA10, ATXN10-related ataxia

ATXN10 Gene Spinocerebellar ataxia type 10, autosomal dominant 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 3-4 weeks. Free home collection in 300+ cities across India.

Genetic TestAdults🏠 Home Collection

✍️ Written By

🩺 Medically Reviewed By

Dr SULOCHANA HEMCHANDRA HOLLA

Dr SULOCHANA HEMCHANDRA HOLLA

Consultant Medical Geneticist · Reg: 8532

Last reviewed: September 7, 2026

Overview

The purpose of the ATXN10 Gene Spinocerebellar ataxia type 10 NGS Genetic Test is to detect mutations in the ATXN10 gene that are associated with SCA10. This test helps in confirming diagnosis, assessing carrier status, and informing family planning decisions.

Test Code
4566
Price
₹20,000
Sample Type
Blood or Extracted DNA or One drop Blood on FTA Card
Result Time
3-4 weeks
Fasting Required
No
Method
NGS Technology
Step 1

Sample Collection

No special preparation required. Provide clinical history and family pedigree.

Method: Venipuncture for blood; Saliva collection for DNA

Step 2

Laboratory Analysis

Blood sample will be collected via venipuncture, or saliva sample using a collection kit.

Step 3

Report Delivery

Apply pressure to the puncture site to stop bleeding. Keep the sample at room temperature for stability.

Timeline: 3-4 weeks

Patient Instructions

1
Before the Test:Provide detailed clinical history and family pedigree during genetic counseling.
2
During the Test:Sample collection will be performed by a trained phlebotomist or using a saliva kit.
3
After the Test:Results will be available in 3-4 weeks. Genetic counseling is recommended for result interpretation.

About This Test

Who Should Get This Test

The purpose of the ATXN10 Gene Spinocerebellar ataxia type 10 NGS Genetic Test is to detect mutations in the ATXN10 gene that are associated with SCA10. This test helps in confirming diagnosis, assessing carrier status, and informing family planning decisions.

How to Prepare

  • Ensure proper patient identification
  • Use sterile collection equipment
  • Label samples correctly
  • Transport samples as per guidelines

Doctor's Notes

Reviewed by — MBBS, MD (Medical Genetics) · Reg. No. 8532

"Genetic testing for SCA10 is essential for accurate diagnosis and genetic counseling. If you have a family history or symptoms, consult a neurologist for evaluation."

Last medically reviewed: September 7, 2026

Test Parameters & Specifications

Sample TypeBlood or Extracted DNA or One drop Blood on FTA Card
Sample Volume5 mL blood
ContainerEDTA tube or FTA Card
Collection MethodVenipuncture for blood; Saliva collection for DNA

Sample Stability

Blood sample stable for 48 hours at room temperature
Extracted DNA stable for longer periods if stored properly
Sample Rejection Criteria:
  • Hemolyzed or clotted blood sample
  • Insufficient sample volume
  • Incorrect sample labeling
  • Contaminated sample

Understanding Your Results

Results from the ATXN10 Gene SCA10 Genetic Test indicate the presence or absence of mutations in the ATXN10 gene. Interpretation should be done by a geneticist or neurologist.
Positive: Pathogenic mutation detected, consistent with SCA10 diagnosis.
Negative: No pathogenic mutation detected, reducing likelihood of SCA10.
Variant of Uncertain Significance (VUS): Further testing and clinical correlation recommended.
⚠️ When to Consult a Doctor:

If the test result is positive or if you have symptoms of SCA10, consult a neurologist for comprehensive evaluation and management.

Limitations

  • ⚠May not detect all types of mutations
  • ⚠Requires genetic counseling for interpretation
  • ⚠Results should be correlated with clinical findings

Risks & Considerations

  • ●Minimal risk from blood draw, such as bruising or infection
  • ●Psychological impact of genetic results

Interfering Factors

  • ●Sample contamination
  • ●Degraded DNA
  • ●Improper sample storage

Compare With Similar Tests

TestATXN10 Gene Spinocerebellar ataxia type 10, autosomal dominant NGS Genetic TestSCA1 Genetic TestSCA2 Genetic TestSCA3 Genetic TestGeneral Ataxia Panel
ComparisonATXN10 Gene Spinocerebellar ataxia type 10, autosomal dominant NGS Genetic Test

Frequently Asked Questions

What is the ATXN10 Gene SCA10 Genetic Test?
This test uses Next Generation Sequencing (NGS) to detect mutations in the ATXN10 gene, which causes Spinocerebellar ataxia type 10 (SCA10), a hereditary neurological disorder.
Who should take this test?
Individuals with a family history of SCA10, symptoms of ataxia such as coordination problems, or those seeking genetic counseling for hereditary ataxia.
How is the test performed?
A blood or saliva sample is collected and analyzed using NGS technology to identify mutations in the ATXN10 gene.
What is the cost of the test?
The test costs INR 20000.0, with free home sample collection available across India.
Is home sample collection available?
Yes, DNA Labs India offers free home sample collection for this test in numerous cities across India.
How long does it take to get results?
Results are typically available within 3 to 4 weeks after sample collection.
What do the results mean?
Results indicate whether a pathogenic mutation in the ATXN10 gene is detected, which can confirm SCA10 diagnosis. Genetic counseling is recommended for interpretation.
Is genetic counseling required?
Yes, genetic counseling is advised before and after testing to understand implications, results, and family risk.
Can this test be used for prenatal diagnosis?
In families with known mutations, prenatal testing may be possible. Consult a genetic counselor for options.
What are the symptoms of SCA10?
Symptoms include coordination problems, difficulty walking, slurred speech, vision issues, tremors, and muscle stiffness, typically appearing in midlife.
Is there a cure for SCA10?
Currently, there is no cure for SCA10, but treatments like physical therapy and medications can help manage symptoms.
How accurate is the test?
The test is highly accurate for detecting known mutations in the ATXN10 gene using NGS technology, but may not detect all mutation types.
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.

Related Tests

Angelman Syndrome Test

₹10,000

Duchenne / Becker Muscular Dystrophy (DMD / BMD) Gene Mutation Test

₹14,000

Episodic Ataxia Type 1 Hotspot Test

₹11,500

Episodic Ataxia Comprehensive Profile Hotspot Test

₹16,000

Megalencephalic Leukoencephalopathy with Subcortical Cysts Van Der Knaap and Nalband MLC Gene Hotspot Mutation Test

₹7,500

Analyzer 18 SMA 18 Test Panel

₹1,755
For Hospitals & Clinics

Reference 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.

LIMS Integration

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.

🧬

Quick Connect

Enter your mobile number and we’ll connect you with the team.

+91

✅ Connecting you now...

🔒 Your number is used to respond to this request.