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Medical information Clinical review pending

Infection Testing

SARS-CoV-2 Antigen Rapid Test

The SARS-CoV-2 Antigen Rapid Test detects active COVID-19 infections quickly. This test is suitable for individuals experiencing symptoms or recent exposure.

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
Nasopharyngeal swab.
Results
Results are typically available within the same day. Confirm with the laboratory before booking.
Preparation
No specific preparation is required for this test. Inform the phlebotomist of any symptoms you are experiencing.
Test priceKSh 2,808

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 SARS-CoV-2 Antigen Rapid 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.

  • ✓Individuals experiencing symptoms consistent with COVID-19 (e.g., fever, cough, loss of taste/smell).
  • ✓Individuals with known close contact exposure to a confirmed COVID-19 case.
  • ✓Screening in specific settings as recommended by public health guidelines.
  • ✓Rapid diagnosis to facilitate timely isolation and treatment.
02

In plain language

What this test helps you understand

This test helps identify individuals currently infected with SARS-CoV-2, aiding in infection control and guiding clinical management.
The SARS-CoV-2 Antigen Rapid Test is a diagnostic tool used to detect the presence of the SARS-CoV-2 virus, the cause of COVID-19. It works by identifying specific viral proteins (antigens) in a sample taken from your nose or throat. This test provides results relatively quickly, aiding in the timely management of potential infections.

This test is particularly useful for identifying individuals who are currently infected and potentially contagious. It uses a rapid chromatographic immunoassay method for fast and reliable detection of SARS-CoV-2 antigens.

Understanding Your Results

A positive result suggests the presence of the virus. If you test positive, it is important to consult a healthcare provider for guidance on next steps, such as isolation and further care.

A negative result means that antigens were not detected in the sample. However, a negative result does not completely rule out a COVID-19 infection, especially if you have symptoms. False negatives can occur. If symptoms persist or you have concerns, consult your doctor for further evaluation or testing.
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. Inform the phlebotomist of any symptoms you are experiencing.
SampleNasopharyngeal swab.
MethodologyRapid Chromatographic Immunoassay.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects antigens, which are typically present when a person is most infectious. However, antigen tests may be less sensitive than molecular tests (like PCR) in detecting very low levels of the virus. False negative results are possible, particularly in individuals with low viral loads or asymptomatic infections. A negative result does not rule out COVID-19.
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

Antigen tests are generally accurate, especially when performed on individuals with symptoms. However, they may be less sensitive than PCR tests, meaning they might miss some infections, particularly those with low viral loads. False negatives can occur.
A positive result indicates that SARS-CoV-2 antigens were detected in your sample, suggesting an active infection. You should follow public health guidelines and consult a healthcare provider.
A negative result means that antigens were not detected. However, it does not completely rule out infection, especially if you have symptoms. Consult your doctor if symptoms persist.
The sample collection involves a swab inserted into the nose or throat, which may cause brief discomfort but is generally not painful.
Results are typically available within the same day. Please confirm the exact turnaround time with the laboratory 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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