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Medical information Clinical review pending

Gynecological Testing

Chromotouch Chromosome SNP Microarray Optima Prenatal Test

The Chromotouch Chromosome SNP Microarray Optima Prenatal Test is a genetic screening test for expectant mothers to detect potential chromosomal abnormalities in the fetus early in pregnancy. It uses advanced microarray technology to analyze fetal genetic material.

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
Amniotic fluid (15 mL minimum), Chorionic villus sampling (CVS) (30 mg minimum), or Umbilical cord blood (4 mL minimum in Lavender top (EDTA) tube).
Results
Approximately 10 working days. Confirm with the laboratory before booking.
Preparation
No specific patient preparation is required. Ensure the sample is collected according to laboratory guidelines. Duly filled Genomic Microarray Requisition Form (Form 19) & Consent form (Form 18) for Prenatal genetic testing are mandatory.
Test priceKSh 37,000

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 Chromotouch Chromosome SNP Microarray Optima Prenatal 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.

  • ✓Advanced maternal age (typically 35 years or older)
  • ✓Family history of chromosomal abnormalities or genetic disorders
  • ✓Abnormal findings on prenatal ultrasound
  • ✓Previous child with a chromosomal abnormality
  • ✓Known parental chromosomal abnormality
  • ✓Carrier status for certain genetic conditions
02

In plain language

What this test helps you understand

This test helps identify chromosomal abnormalities in a fetus, providing information for pregnancy management and potential interventions. It offers a more detailed analysis than standard screening tests.
The Chromotouch Chromosome SNP Microarray Optima Prenatal Test is a state-of-the-art genetic testing method designed to assess the genetic health of an unborn child. This test is valuable for identifying potential chromosomal abnormalities early in pregnancy, allowing for informed decisions and appropriate management if needed.

This test utilizes advanced microarray technology to analyze the genetic material from the fetus, providing a comprehensive look at chromosomal structure. It can detect abnormalities that may not be visible on standard ultrasound scans.

This test is particularly relevant for expectant mothers who may have increased risk factors, such as advanced maternal age, a family history of genetic disorders, abnormal ultrasound findings, or known carrier status for genetic mutations.

Early detection of potential genetic disorders offers several benefits, including the opportunity for informed decision-making regarding pregnancy management, access to specialized care and support, and peace of mind for expectant parents.

Results are typically available within 10 working days. A genetic counselor or healthcare provider will be available to discuss the results, explain any findings, and guide you through potential 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 →
PreparationNo specific patient preparation is required. Ensure the sample is collected according to laboratory guidelines. Duly filled Genomic Microarray Requisition Form (Form 19) & Consent form (Form 18) for Prenatal genetic testing are mandatory.
SampleAmniotic fluid (15 mL minimum), Chorionic villus sampling (CVS) (30 mg minimum), or Umbilical cord blood (4 mL minimum in Lavender top (EDTA) tube).
MethodologyFluorescence In Situ Hybridization (FISH) and Single Nucleotide Polymorphism (SNP) microarray analysis.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test detects common chromosomal abnormalities but may not detect all genetic conditions. It does not provide information about single gene disorders unless specifically requested. 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 detects chromosomal abnormalities, such as aneuploidies (extra or missing chromosomes) and microdeletions/microduplications (small missing or extra pieces of chromosomes).
This test is considered a diagnostic test, meaning it can confirm or rule out specific chromosomal abnormalities.
This test can typically be performed after 10 weeks of gestation using CVS or amniocentesis.
A genetic counselor or your doctor will discuss the results with you, explain their meaning, and discuss any potential follow-up steps.
Sample collection methods like amniocentesis and CVS carry small risks. Discuss these risks thoroughly with your healthcare provider.
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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