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Medical information Clinical review pending

Genetic Testing

Comprehensive Immuno Panel Genetic Test

The Comprehensive Immuno Panel NGS Genetic DNA Test uses advanced Next Generation Sequencing (NGS) technology to analyze genetic variations associated with immune system function. This test helps identify potential genetic predispositions to immunological disorders, aiding in 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). Confirm specific requirements with the laboratory before booking.
Results
3 to 4 weeks. Confirm with the laboratory before booking.
Preparation
No special preparation is required for this test. Confirm with the laboratory before booking.
Test priceKSh 40,000

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 Comprehensive Immuno Panel Genetic 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.

  • ✓Family history of immunological disorders
  • ✓Frequent or severe infections
  • ✓Diagnosis of autoimmune conditions
  • ✓Unexplained allergies
  • ✓Chronic inflammation
  • ✓Suspected primary immunodeficiency
  • ✓Genetic counseling for immune-related conditions
02

In plain language

What this test helps you understand

Identifies genetic predispositions to immunological disorders, including autoimmune diseases and immunodeficiencies. Aids in diagnosis and personalized treatment planning based on genetic insights. Helps understand family health risks.
The Comprehensive Immuno Panel NGS Genetic DNA Test is an advanced diagnostic tool designed to evaluate genetic predispositions to various immunological disorders. By utilizing Next Generation Sequencing (NGS) technology, this test allows for a comprehensive analysis of genetic markers associated with immune system function. It is essential for individuals who may be at risk for hereditary immune disorders, providing valuable information that can guide medical decisions and treatment plans.

This test evaluates numerous genes related to immune function, including those associated with conditions such as autoimmune diseases, immunodeficiencies, and other related disorders. By identifying specific genetic mutations or variations, healthcare providers can better understand a patient's risk profile and tailor their treatment accordingly.

Individuals with a family history of immunological disorders or those experiencing symptoms such as frequent infections, autoimmune conditions, unexplained allergies, or chronic inflammation should consider this test. It is particularly beneficial for patients who have undergone genetic counseling or have a clinical history suggestive of immune system dysfunction.

Benefits of taking this test include identifying genetic predispositions, facilitating personalized treatment plans, enhancing understanding of family health history, and providing valuable insights for patients and their families. Results are typically available within 3 to 4 weeks and should be discussed with a healthcare provider to understand their implications and guide any necessary 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 →
PreparationNo special preparation is required for this test. Confirm with the laboratory before booking.
SampleBlood sample (EDTA tube). Confirm specific requirements with the laboratory before booking.
MethodologyNext Generation Sequencing (NGS) of relevant genes associated with immune function.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test identifies specific genetic variations but does not guarantee the development of a disorder. Results may not cover all possible genetic causes of immunological conditions. Interpretation requires clinical correlation.
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 analyzes genes related to immune system function to identify genetic variations associated with immunological disorders like autoimmune diseases and immunodeficiencies.
Individuals with a family history of immune disorders, frequent infections, autoimmune conditions, or other symptoms suggestive of immune system dysfunction may benefit from this test.
Results should be interpreted by a qualified healthcare provider in the context of your medical history and clinical presentation.
A blood sample is required for this test. Please confirm specific collection details with the laboratory.
The typical turnaround time is 3 to 4 weeks, but this can vary. Confirm the current turnaround time with the laboratory.
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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