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Medical information Clinical review pending

Genetic Testing

Oxford Nanopore 1GB

The Oxford Nanopore 1GB test provides comprehensive DNA sequencing to identify genetic variations and predispositions. This advanced genetic analysis offers valuable insights for personalised healthcare.

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
Confirm with the laboratory before booking.
Results
Approximately 4 weeks. Confirm with the laboratory before booking.
Preparation
Confirm with the laboratory before booking.
Test priceKSh 130,000

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 Oxford Nanopore 1GB 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 genetic disorders
  • ✓Unexplained health issues
  • ✓Understanding genetic risks for specific diseases
  • ✓Family planning and genetic risk assessment
02

In plain language

What this test helps you understand

Identifies genetic variations and predispositions. Supports personalised healthcare approaches. Aids in understanding potential genetic risks.
The Oxford Nanopore 1GB test is a cutting-edge genetic testing method that allows for comprehensive DNA sequencing. This advanced technology is crucial for identifying genetic variations and understanding an individual's genetic predisposition to various conditions. By analyzing the extracted DNA sample, healthcare professionals can gain insights into a patient's genetic makeup, allowing for personalized medical approaches. Understanding your genetic makeup can empower you and your doctor to make informed decisions about your health.
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 →
PreparationConfirm with the laboratory before booking.
SampleConfirm with the laboratory before booking.
MethodologyOxford Nanopore DNA sequencing technology.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test identifies genetic variations but does not predict future health outcomes with certainty. Results should be interpreted by a qualified healthcare professional.
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

This test measures and detects variations in your DNA sequence, which can provide insights into genetic disorders or predispositions to certain diseases.
Individuals with a family history of genetic disorders, those with unexplained health issues, or people seeking to understand their genetic risks may benefit from this test.
It is essential to consult with a healthcare professional to interpret your results accurately and understand their implications for your health.
Yes, the test is available at our branches in Nairobi, Mombasa, Kisumu, and other locations. Please contact us for specific availability.
The current discounted price is 130,000 KSh. The regular price is 170,000 KSh. Please confirm the current price when booking.
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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