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Medical information Clinical review pending

Genetic Testing

HSV 1 2 DNA Detection RNA Detection Qualitative Test

Detects the presence of Herpes Simplex Virus types 1 and 2 (HSV-1 and HSV-2) using Real Time PCR technology. Helps confirm active infection and differentiate between virus types.

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
Whole Blood, Serum, Plasma, Cerebrospinal Fluid (C.S.F), Genital Swabs. Confirm specific sample type needed with the laboratory before booking.
Results
Results typically available within 36 hours via email and 24 hours via phone. Confirm exact turnaround time with the laboratory before booking.
Preparation
No special preparation is required for this test. However, inform the laboratory about any medications you are currently taking. Follow specific instructions provided by the collecting physician or laboratory.
Test priceKSh 12,000

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 HSV 1 2 DNA Detection 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.

  • ✓Symptoms suggestive of herpes (e.g., sores, blisters).
  • ✓History of sexually transmitted infections.
  • ✓Individuals with compromised immune systems.
  • ✓Pregnant women assessing risk of neonatal transmission.
  • ✓Confirmation of suspected herpes infection.
  • ✓Differentiation between HSV-1 and HSV-2.
02

In plain language

What this test helps you understand

This test is used to detect the presence of HSV-1 and HSV-2 DNA and RNA, aiding in the diagnosis of active herpes simplex virus infections and differentiating between the two types.
The HSV 1 2 DNA Detection RNA Detection Qualitative Test is a diagnostic tool used to identify the presence of Herpes Simplex Virus types 1 and 2 (HSV-1 and HSV-2) in the body. This test uses Real Time PCR technology for rapid and accurate detection of viral DNA and RNA. Understanding your HSV status is important for managing symptoms and preventing transmission.

This test measures the presence of HSV-1 and HSV-2 DNA and RNA in samples like whole blood, serum, plasma, cerebrospinal fluid (C.S.F), and genital swabs. It helps confirm an active infection and distinguish between the two types of herpes viruses.

Individuals experiencing symptoms like sores or blisters, those with a history of sexually transmitted infections, people with weakened immune systems, and pregnant women may benefit from this test.

Taking this test provides an accurate diagnosis, guides treatment and management, helps prevent transmission to others, and offers peace of mind.

Results are typically available within 36 hours via email and 24 hours via phone. A positive result indicates an active infection, while a negative result suggests no detectable virus. Discuss your results with a healthcare provider for proper interpretation and next steps.
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 special preparation is required for this test. However, inform the laboratory about any medications you are currently taking. Follow specific instructions provided by the collecting physician or laboratory.
SampleWhole Blood, Serum, Plasma, Cerebrospinal Fluid (C.S.F), Genital Swabs. Confirm specific sample type needed with the laboratory before booking.
MethodologyReal Time PCR (Polymerase Chain Reaction).
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects the presence of viral DNA/RNA, indicating an active infection. It may not detect latent infections. False negatives can occur if the viral load is very low or if the sample is collected improperly. False positives are rare but possible. 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

This test detects the genetic material (DNA and RNA) of Herpes Simplex Virus types 1 and 2 (HSV-1 and HSV-2).
This test is designed to detect an active infection, as it looks for the presence of the virus's genetic material.
Samples can include whole blood, serum, plasma, cerebrospinal fluid (C.S.F), or genital swabs. Your doctor will advise on the appropriate sample.
Results are typically available within 36 hours via email and 24 hours via phone, but confirm the exact time with the laboratory.
A positive result indicates that the virus's genetic material was detected, suggesting an active infection. Discuss the implications with your healthcare provider.
Generally, no special preparation is needed. Inform the lab about any medications you are taking.
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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