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Medical information Clinical review pending

Genetic Testing

Liquid Biopsy 117 Gene Panel

The Liquid Biopsy 117 Gene Panel is an advanced genetic test analyzing 117 genes from a blood sample to detect mutations associated with various genetic disorders. It aids in early diagnosis and personalized treatment planning.

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
Blood sample (EDTA tube).
Results
Approximately 25 working days. Confirm with the laboratory before booking.
Preparation
Confirm with the laboratory before booking. A doctor’s prescription is required. This test is not applicable for individuals undergoing surgery, those who are pregnant, or people planning to travel abroad.
Test priceKSh 66,000

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 Liquid Biopsy 117 Gene Panel 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 symptoms potentially related to genetic conditions
  • ✓Assessment of genetic risk factors
  • ✓Guiding personalized treatment strategies
  • ✓Monitoring disease progression (Confirm with the laboratory before booking.)
02

In plain language

What this test helps you understand

Detects genetic mutations in 117 genes from a blood sample. Aids in early diagnosis and personalized treatment planning for various genetic disorders.
The Liquid Biopsy 117 Gene Panel is a revolutionary diagnostic tool that allows for the non-invasive analysis of genetic material found in the blood. This advanced test is designed to detect mutations across 117 specific genes associated with various genetic disorders, providing crucial information for early diagnosis and tailored treatment strategies. Unlike traditional biopsies, this method minimizes discomfort and risk, making it an ideal option for patients.

This test measures the presence of genetic mutations in the blood, specifically focusing on 117 genes that are critical for understanding genetic predispositions to certain diseases. By identifying these mutations, healthcare providers can make informed decisions regarding patient care.

Individuals who may benefit from the Liquid Biopsy 117 Gene Panel include those with a family history of genetic disorders, patients experiencing unexplained symptoms that may suggest a genetic condition, and individuals seeking information on their genetic risk factors for various diseases.

Key benefits include a non-invasive testing method, early detection of genetic mutations allowing for timely intervention, personalized treatment options based on individual genetic profiles, and convenient sample collection via a simple blood draw.

Results are typically available within approximately 25 working days. It is essential to discuss your results with a qualified healthcare professional who can provide guidance on the implications of any detected mutations and recommend appropriate follow-up actions.
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. A doctor’s prescription is required. This test is not applicable for individuals undergoing surgery, those who are pregnant, or people planning to travel abroad.
SampleBlood sample (EDTA tube).
MethodologyNext-Generation Sequencing (NGS) on circulating tumor DNA (ctDNA) or cell-free DNA (cfDNA) from a blood sample.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects specific mutations in the 117 genes analyzed. It may not detect all possible genetic mutations or all types of genetic disorders. Results should be interpreted in conjunction with clinical findings and other diagnostic tests.
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

A liquid biopsy is a test performed on a sample of blood to look for cancer cells or pieces of DNA from tumors that are circulating in the blood.
No, this test involves a simple blood draw, which is minimally invasive and generally painless.
Results are reported by the laboratory and should be discussed with your healthcare provider for interpretation and guidance.
Yes, a doctor’s prescription is required to proceed with this test.
Insurance coverage varies. Please check with your insurance provider regarding coverage for this specific test.
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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