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Genetic Testing

SCA1 Spinocerebellar Ataxia ATXN1 Gene Mutation Test

The SCA1 Spinocerebellar Ataxia ATXN1 Gene Mutation Test helps diagnose Spinocerebellar Ataxia Type 1, a genetic disorder affecting coordination and balance. This test identifies mutations in the ATXN1 gene.

General information only: This page is not a diagnosis or personal medical advice. A qualified clinician should decide whether testing is appropriate and interpret results in context.

Review status: No completed medical review is recorded for this page.

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Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
4 mL (2 mL minimum) of whole blood collected in a Lavender top (EDTA) tube.
Results
Results are typically available within 10-12 days. Confirm with the laboratory before booking.
Preparation
No specific patient preparation is required for this blood test. Confirm with the laboratory before booking.
Test priceKSh 5,850

Payment: M-Pesa and card options can be confirmed during booking.

Insurance & government schemes

Is this test covered for you?

We help you verify whether the SCA1 Spinocerebellar Ataxia ATXN1 Gene Mutation Test test can be claimed against your insurer, employer scheme or a Kenyan government health scheme — before you book. Coverage depends on your plan, clinical indication and your provider's rules; final approval always rests with them.

Talk to a claims advisor

Providers & schemes we can help you check

Government & public schemes

SHIF — Social Health Insurance Fund Linda Mama EduAfya NHIF (legacy cards)

Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.

Private insurers & employer schemes

Jubilee Health AAR APA Britam CIC Madison Resolution Pioneer Minet Old Mutual GA Life Heritage + other licensed insurers

Names shown for identification only — listing does not imply partnership or guarantee of coverage.

Have these ready when we check

  • Insurer or scheme name & policy / member number
  • A clinician's request / prescription for the test
  • Pre-authorisation letter, if your plan requires one

Free coverage check

Ask us to verify your cover

Send your details and our claims team confirms what documents you need and whether pre-authorisation applies — usually the same working day.

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Used only to process your coverage check — see our Privacy Policy. Verification support is free and does not guarantee your provider will pay.

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01

Start with fit

Is this the right test for you?

The best test starts with a clear clinical question. These are common reasons a clinician or family may consider this test.

  • ✓Symptoms of ataxia (e.g., unsteady gait, dizziness, difficulty with fine motor skills)
  • ✓Family history of Spinocerebellar Ataxia
  • ✓Progressive neurological symptoms suggestive of SCA1
  • ✓Differential diagnosis of cerebellar ataxia
02

In plain language

What this test helps you understand

This test aids in the diagnosis of Spinocerebellar Ataxia Type 1 (SCA1) by detecting mutations in the ATXN1 gene. A confirmed diagnosis allows for appropriate patient management, genetic counseling for the individual and family, and informed decisions regarding treatment and potential clinical trial participation.
The SCA1 Spinocerebellar Ataxia ATXN1 Gene Mutation Test is a diagnostic tool used to identify Spinocerebellar Ataxia Type 1 (SCA1). SCA1 is a genetic disorder characterized by the progressive degeneration of the cerebellum, leading to difficulties with coordination, balance, and movement. This test specifically looks for mutations within the ATXN1 gene, which are the underlying cause of SCA1. Understanding the genetic basis of the condition is important for accurate diagnosis, management, and genetic counseling. This test can provide crucial information for individuals experiencing symptoms suggestive of SCA1 or those with a family history of the disorder.
03

Medical review status

Clinical review pending

A completed medical review is not recorded for this page. No clinician has endorsed the information shown here. Please discuss testing decisions with a qualified healthcare professional.

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04

A simple process

What happens next?

You do not have to navigate the test alone. We help you move from question to next step.

1

Speak with us

We check the test and answer your questions before collection.

2

Give your sample

Choose home collection or a coordinated hub visit in Kenya. We explain whether this test uses a cheek swab or blood draw.

3

Understand your report

A counselor helps you understand the result and the next steps.

05

Choose your collection

Home collection or a lab visit

We will explain the sample, preparation, and next steps before anything is collected.

Home collection

Choose a coordinated visit at home or another convenient location. Our team confirms the appointment and sample requirements in advance.

Lab or hub visit

Prefer to visit a coordinated location? We can guide you to the right hub and explain what to expect when you arrive.

Ask about locations →
PreparationNo specific patient preparation is required for this blood test. Confirm with the laboratory before booking.
Sample4 mL (2 mL minimum) of whole blood collected in a Lavender top (EDTA) tube.
MethodologyGenetic analysis techniques are used to detect mutations in the ATXN1 gene. Confirm with the laboratory before booking.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test specifically targets mutations in the ATXN1 gene. It will not detect mutations in other genes that can cause Spinocerebellar Ataxia or other neurological disorders. A negative result does not completely rule out SCA1 or other forms of ataxia. Confirm with the laboratory before booking.
06

Read your report

What common result terms mean

PositiveA finding was identified. Your clinician or counselor will explain what it means for your care.
NegativeThe specific finding tested for was not identified. It does not rule out every possible cause.
VUSA variant was found, but current evidence is not enough to classify it. Your counselor can explain follow-up.
07

Questions people ask

Frequently asked questions

SCA1 is a genetic disorder that causes progressive problems with movement, coordination, and balance due to damage to the cerebellum.
Individuals experiencing symptoms like unsteady gait, dizziness, or difficulty with coordination, especially if there is a family history of similar conditions, should consult a doctor about testing.
A positive result indicates the presence of a mutation in the ATXN1 gene associated with SCA1. It is important to discuss this result with your healthcare provider for interpretation and guidance.
A negative result means no mutation in the ATXN1 gene was detected. Your doctor will discuss potential reasons for your symptoms and may recommend further investigation.
Insurance coverage varies. Please check with your insurance provider regarding coverage for genetic testing.
The test requires a blood sample, which can be collected at one of our branches or through our home sample collection service.
08

Collaboration

Open for partnership with hospitals, clinics, doctors & researchers

Whether you are referring patients, building a research programme or supporting students, we work as an extension of your team — with responsive communication and clear scientific standards.

Hospitals & clinics

Referral pathways, coordinated sample logistics and shared reporting that fits your clinical workflow.

Doctors & specialists

LOINC-coded reports, ACMG-based variant classification and a direct scientific line for complex cases.

Research institutions

Sanger sequencing, NGS panels and custom assays — with project design support, batch pricing and agreed turnaround commitments.

Students & academic projects

Discounted laboratory services for college, master's and PhD research projects — including proposal guidance and cost-effective batch testing.

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09

Trust & transparency

Sources, standards & how this page is maintained

Standards & references

  • ACMG/AMP technical standards for sequence variant interpretation
  • ClinGen curation and gene–disease validity frameworks where applicable
  • LOINC-coded reporting for interoperable results
  • ISO 9001:2015 quality management; ISO 15189 accreditation in progress

Page provenance

  • Last updated: September 27, 2026
  • Medical review: not yet completed
  • Written for patients & clinicians in Kenya; reviewed periodically against current guidance

Medical disclaimer: this page is general information, not a diagnosis or personal medical advice. Testing decisions and result interpretation should be made with a qualified healthcare professional.

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