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Medical information Clinical review pending

Infection Testing

SARS RNA Detection Qualitative Test

Detects the presence of SARS-CoV-2 RNA to diagnose active COVID-19 infection using Real Time PCR technology. Recommended for symptomatic individuals or those with known 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
Bronchial swab or Bronchial lavage sample.
Results
Results are typically available within 24 hours via phone or 36 hours via email. Confirm with the laboratory before booking.
Preparation
Patients are required to sign a consent document and provide relevant clinical history related to SARS. Confirm with the laboratory before booking.
Test priceKSh 14,875

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 RNA Detection Qualitative 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 suggestive of COVID-19.
  • ✓Individuals with known close contact exposure to a confirmed COVID-19 case.
  • ✓Screening individuals in high-risk settings or populations.
  • ✓Patients with underlying health conditions potentially increasing COVID-19 severity.
  • ✓Confirmation of infection in epidemiological investigations.
02

In plain language

What this test helps you understand

This test is used to confirm an active SARS-CoV-2 infection by detecting viral RNA. It aids in diagnosis, guiding treatment decisions, and implementing appropriate isolation measures to prevent further spread.
The SARS RNA Detection Qualitative Test is a diagnostic tool used to identify the presence of SARS-CoV-2 RNA in patient samples. This test is important for managing and controlling viral infections, particularly COVID-19. It uses Real Time PCR technology to detect the virus in samples collected from bronchial swabs or bronchial lavage.

This test specifically measures the presence of RNA from the SARS-CoV-2 virus. Detecting this viral RNA helps healthcare providers confirm an active infection, which is crucial for timely treatment and isolation measures.

This test is recommended for individuals showing symptoms of COVID-19 (like fever, cough, difficulty breathing), those who have been in close contact with confirmed cases, and people with underlying health conditions that might increase their risk of severe illness.

Benefits of this test include early detection of COVID-19, enabling prompt isolation and treatment, providing peace of mind, and contributing to public health efforts by identifying and controlling outbreaks.

Results are typically available within 36 hours via email or 24 hours via phone. A positive result indicates an active infection. A negative result suggests the virus was not detected in the sample. Discuss your results with a healthcare provider for appropriate guidance.

We have branches across Kenya, including Nairobi, Mombasa, and Kisumu. Home sample collection services are also available. To book the test, please call or WhatsApp us at +254711564616. Before the test, patients must sign a consent document and provide relevant clinical history related to SARS.
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 →
PreparationPatients are required to sign a consent document and provide relevant clinical history related to SARS. Confirm with the laboratory before booking.
SampleBronchial swab or Bronchial lavage sample.
MethodologyReal Time Polymerase Chain Reaction (PCR).
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This is a qualitative test, meaning it detects the presence or absence of viral RNA but does not quantify the amount. False negatives can occur if the sample is collected improperly, too early in the infection, or if the viral load is very low. False positives are rare but possible due to contamination. This test detects current infection, not past exposure or immunity.
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 detects the genetic material (RNA) of the SARS-CoV-2 virus, which causes COVID-19.
Real Time PCR is highly accurate for detecting active infection. However, accuracy depends on proper sample collection and timing relative to infection. Confirm with the laboratory before booking.
If you test positive, you should isolate yourself immediately and follow the guidance provided by your healthcare provider and local public health authorities.
A negative result means the virus was not detected in the sample at the time of testing. However, it does not completely rule out infection, especially if symptoms persist or exposure was recent. Consult your doctor.
Confirm with the laboratory before booking.
Yes, home sample collection services are available. Please call or WhatsApp us at +254711564616 to arrange.
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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