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Medical information Clinical review pending

Infection Testing

Mycoplasma Genitalium RNA Detection Qualitative Test

Detects the presence of Mycoplasma Genitalium RNA, a bacterium causing STIs. This qualitative test uses Real Time PCR for accurate diagnosis of reproductive health issues. Confirm price and turnaround time before booking.

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
Urethra or vaginal swab, cell culture, cervical discharge, rectum swab, blood, or urine. Confirm specific sample type needed with the laboratory before booking.
Results
Confirm turnaround time with the laboratory before booking. The source indicates a turnaround time of 4 working days.
Preparation
Patients need to sign a consent document. Providing relevant clinical history for Mycoplasma Genitalium testing is recommended. Confirm specific preparation instructions with the laboratory before booking.
Test priceKSh 11,900

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 Mycoplasma Genitalium 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 of sexually transmitted infections (STIs)
  • ✓Unusual genital discharge or pain
  • ✓History of STIs
  • ✓Multiple sexual partners
  • ✓Unexplained infertility
  • ✓Recurrent urinary tract infections
  • ✓Routine sexual health screening
02

In plain language

What this test helps you understand

This test helps diagnose Mycoplasma Genitalium infections, which can cause significant reproductive health issues if left untreated. Accurate detection guides appropriate treatment decisions.
The Mycoplasma Genitalium RNA Detection Qualitative Test is a diagnostic tool used to identify the presence of Mycoplasma Genitalium, a bacterium known to cause sexually transmitted infections (STIs). This test is important for individuals experiencing symptoms related to reproductive health or those concerned about STI risk. Early detection allows for appropriate treatment, helping to prevent potential complications and protect overall health.

This test specifically looks for the RNA of Mycoplasma Genitalium in samples like swabs from the urethra or vagina, cervical discharge, rectal swabs, blood, or urine. Using Real Time PCR technology, the test provides reliable results to aid in diagnosis.

Consider this test if you are experiencing unusual genital symptoms like discharge or pain, have a history of STIs, have multiple sexual partners, or are experiencing unexplained infertility or recurrent urinary tract infections. It can also be part of routine sexual health screening for sexually active individuals.

Benefits of this test include accurate diagnosis, guidance on treatment, prevention of complications from untreated infections, and peace of mind regarding your sexual health.

Your healthcare provider will interpret your results. A positive result indicates the presence of the bacterium, while a negative result suggests it is not detected. Discuss the results with your doctor to determine the next steps, which may include treatment or further investigation.
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 need to sign a consent document. Providing relevant clinical history for Mycoplasma Genitalium testing is recommended. Confirm specific preparation instructions with the laboratory before booking.
SampleUrethra or vaginal swab, cell culture, cervical discharge, rectum swab, blood, or urine. 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 is a qualitative test, meaning it detects the presence or absence of Mycoplasma Genitalium RNA but does not quantify the amount. False negatives can occur if the sample is collected improperly or if the bacterial load is very low. False positives are rare but possible. Confirm limitations 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

Mycoplasma Genitalium is a type of bacteria that can cause sexually transmitted infections (STIs), potentially leading to conditions like urethritis, cervicitis, and pelvic inflammatory disease.
Early detection of Mycoplasma Genitalium allows for timely treatment, which can prevent serious complications and long-term health issues related to untreated STIs.
Various samples can be used, including swabs from the urethra or vagina, cervical discharge, rectal swabs, blood, or urine. The specific sample required should be confirmed with the laboratory.
The Real Time PCR method used for this test is highly accurate for detecting the presence of Mycoplasma Genitalium RNA. However, like all tests, factors like sample quality can influence results.
You should discuss your results with your healthcare provider. They will interpret the findings and recommend appropriate next steps, such as treatment if the test is positive.
Yes, laboratory testing is conducted with strict confidentiality protocols to protect patient privacy.
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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