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Medical information Clinical review pending

Genetic Testing

CD27 Gene Lymphoproliferative Syndrome Type 2 Genetic Test

This genetic test identifies mutations in the CD27 gene associated with lymphoproliferative disorders. It uses Next Generation Sequencing (NGS) technology to analyze DNA and help understand potential risks related to immune system function. Confirm with the laboratory 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
Blood sample, Extracted DNA, or One drop of blood on FTA Card.
Results
Confirm with the laboratory before booking.
Preparation
A clinical history evaluation and genetic counseling session, including a pedigree chart of affected family members, are recommended before the test.
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 CD27 Gene Lymphoproliferative Syndrome Type 2 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 lymphoproliferative disorders
  • ✓Symptoms suggestive of immune system dysfunction
  • ✓Unexplained fevers, night sweats, or swollen lymph nodes
  • ✓Diagnosis of suspected lymphoproliferative syndrome
  • ✓Genetic counseling for individuals with related conditions
02

In plain language

What this test helps you understand

Identifies mutations in the CD27 gene associated with lymphoproliferative disorders, aiding in risk assessment and management.
The CD27 Gene Lymphoproliferative Syndrome Type 2 NGS Genetic DNA Test is a diagnostic tool used to identify genetic mutations linked to lymphoproliferative disorders. Understanding genetic predisposition is important for managing potential health issues. This test uses Next Generation Sequencing (NGS) technology for precise analysis of the CD27 gene.

This genetic test specifically looks for mutations in the CD27 gene, which plays a role in regulating the immune system. By analyzing a DNA sample, the test can identify abnormalities that might increase the risk of lymphoproliferative syndromes, conditions related to the abnormal growth of lymphocytes.

Individuals who might consider this test include those with a family history of lymphoproliferative disorders, patients experiencing symptoms like unexplained fevers, night sweats, or swollen lymph nodes, and individuals with known immune system issues.

Taking this test can offer benefits such as early detection of genetic risks, enabling timely intervention and management. It also provides information that can help tailor treatment options and assist families in health-related planning.

Results are provided in a comprehensive report. It is important to discuss these results with a healthcare provider or genetic counselor to fully understand their implications and plan 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 →
PreparationA clinical history evaluation and genetic counseling session, including a pedigree chart of affected family members, are recommended before the test.
SampleBlood sample, Extracted DNA, or One drop of blood on FTA Card.
MethodologyNext Generation Sequencing (NGS) of the CD27 gene.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects specific mutations in the CD27 gene but may not identify all possible genetic variations associated with lymphoproliferative disorders. Results should be interpreted in conjunction with clinical findings.
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 is a condition related to the abnormal growth of lymphocytes, often linked to immune system dysfunction. The CD27 gene plays a role in this process.
Individuals with a family history of related disorders, specific symptoms, or known immune issues may be candidates. Consult your doctor.
The test uses advanced NGS technology for precise analysis. However, it may not detect all possible mutations. Discuss limitations with your healthcare provider.
Results are provided in a report. It is crucial to discuss them with a healthcare provider or genetic counselor to understand their meaning and implications.
Confirm with the laboratory before booking.
Confirm with the laboratory before booking.
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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