Skip to main content
Medical information Clinical review pending

Genetic Testing

Infertility Panel Genetic Test

The Infertility Panel NGS Genetic DNA Test uses advanced sequencing technology to identify genetic factors that may contribute to infertility, aiding couples facing conception challenges.

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.

Ask a question
Counselor guidance included Confidential handling Kenya-wide coordination

At a glance

Plan your test

Sample
Blood sample, extracted DNA, or a single drop of blood on an FTA card.
Results
Results are typically available within 3 to 4 weeks. Confirm with the laboratory before booking.
Preparation
Provide a complete clinical history. A genetic counseling session is recommended to create a family pedigree chart.
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 Infertility 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.

+254

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.

  • ✓Difficulty conceiving after one year of unprotected intercourse
  • ✓History of recurrent miscarriages
  • ✓Known family history of genetic disorders
  • ✓Advanced maternal age
  • ✓Unexplained infertility
  • ✓Previous reproductive health issues
02

In plain language

What this test helps you understand

Identifies genetic factors potentially contributing to infertility, guiding diagnosis and treatment strategies for couples facing conception difficulties.
The Infertility Panel NGS Genetic DNA Test is a cutting-edge diagnostic tool designed to help understand the genetic factors underlying infertility. For couples experiencing difficulties conceiving, this test offers valuable insights that can inform treatment strategies and potentially improve the chances of successful pregnancy.

This test utilizes Next Generation Sequencing (NGS) technology to analyze specific genetic markers associated with reproductive disorders. It looks for mutations in genes known to impact fertility, providing a comprehensive assessment of potential genetic contributors to infertility.

Individuals or couples facing challenges with conception may benefit from this test. This includes those who have been trying to conceive for a year or more without success, have experienced recurrent miscarriages, or have a family history of genetic disorders. Advanced maternal age, previous reproductive health issues, or unexplained infertility are also reasons to consider this test.

Taking this test can help identify genetic factors affecting fertility, guide appropriate treatment options, provide clarity on potential hereditary issues, and support informed decision-making about reproductive health.

Results are provided in a detailed report. It is crucial to discuss these results with a qualified healthcare provider for accurate interpretation and guidance on next steps.

Our laboratory has branches across Kenya. To book the Infertility Panel NGS Genetic DNA Test, please contact us at +254711564616.
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 →
PreparationProvide a complete clinical history. A genetic counseling session is recommended to create a family pedigree chart.
SampleBlood sample, extracted DNA, or a single drop of blood on an FTA card.
MethodologyNext Generation Sequencing (NGS) technology.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test analyzes specific genes associated with infertility; it may not detect all possible genetic causes. Results should be interpreted in the context of clinical history and other relevant tests. 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 analyzes genetic markers associated with reproductive disorders using Next Generation Sequencing (NGS) to identify potential genetic factors contributing to infertility.
Individuals or couples experiencing difficulty conceiving, recurrent miscarriages, or with a family history of genetic disorders may benefit from this test.
A sample of blood, extracted DNA, or a single drop of blood on an FTA card is required.
Results are typically available within 3 to 4 weeks.
It is essential to consult with a qualified healthcare provider to interpret the results accurately and discuss potential next steps.
You can book the test by calling or WhatsApping us at +254711564616.
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.

Keep exploring

Related tests

View all tests →
Chat on WhatsApp