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Medical information Clinical review pending

Genetic Testing

ASB10 Gene Glaucoma Open Angle Type 1F Genetic Test

Genetic test using Next-Generation Sequencing (NGS) to identify variations in the ASB10 gene associated with open-angle glaucoma. Helps assess risk and inform management.

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
Blood sample (EDTA tube) or Saliva sample. Confirm with the laboratory before booking.
Results
Confirm with the laboratory before booking.
Preparation
No specific preparation is required for this test. Confirm with the laboratory before booking.
Test priceKSh 40,000

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 ASB10 Gene Glaucoma Open Angle Type 1F Genetic 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.

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.

  • ✓Family history of glaucoma
  • ✓Symptoms suggestive of glaucoma (vision loss, eye pain, high intraocular pressure)
  • ✓Individuals over 40, especially those of African descent
  • ✓Assessing genetic predisposition to open-angle glaucoma
02

In plain language

What this test helps you understand

Identifies genetic variations in the ASB10 gene linked to open-angle glaucoma, aiding in risk assessment and personalized management strategies.
The ASB10 Gene Glaucoma Open Angle Type 1F NGS Genetic DNA Test is an advanced diagnostic tool designed to detect genetic mutations associated with glaucoma, a leading cause of irreversible blindness worldwide. This test employs Next-Generation Sequencing (NGS) technology to analyze the ASB10 gene, providing critical insights into the genetic factors that may contribute to the development of glaucoma. This test specifically measures variations in the ASB10 gene that are linked to open-angle glaucoma. By identifying these genetic markers, healthcare providers can better understand an individual’s risk and tailor appropriate monitoring and treatment plans. Understanding your results involves consultation with a qualified ophthalmologist and genetic counselor who will provide guidance on the implications and any necessary follow-up actions. A positive result indicates a higher risk but does not guarantee the development of glaucoma.
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.

Meet the DNA Labs Kenya medical team →
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 preparation is required for this test. Confirm with the laboratory before booking.
SampleBlood sample (EDTA tube) or Saliva sample. Confirm with the laboratory before booking.
MethodologyNext-Generation Sequencing (NGS) analysis of the ASB10 gene.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test analyzes only the ASB10 gene. Glaucoma can be influenced by other genes and environmental factors. A negative result does not completely rule out the risk of developing glaucoma. Results should be interpreted in conjunction with clinical findings.
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

Glaucoma is a group of eye conditions that damage the optic nerve, often associated with high pressure inside the eye. It can lead to vision loss and blindness.
Variations in the ASB10 gene have been linked to an increased risk of developing open-angle glaucoma.
Individuals with a family history of glaucoma, those experiencing symptoms, or those over 40, particularly of African descent, may benefit from this test.
Your results will be reviewed by a qualified ophthalmologist and genetic counselor who will discuss the findings and recommend appropriate next steps.
No, a positive result indicates an increased genetic risk but does not guarantee you will develop glaucoma. Clinical evaluation is still essential.
A sample can be collected via a blood draw or a saliva sample. We offer home collection services for convenience.
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.

Explore partnerships
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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