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Genetic Testing

G6PC Gene Glycogen Storage Disease Type 1A Genetic Test

This genetic test identifies mutations in the G6PC gene associated with Glycogen Storage Disease Type 1A, a metabolic disorder. It uses Next Generation Sequencing (NGS) technology.

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
A blood sample is required for this test. Confirm specific collection requirements with the laboratory before booking.
Results
Results are typically available within 3 to 4 weeks. Confirm the current turnaround time with the laboratory before booking.
Preparation
No special preparation is typically required for this blood test. However, confirm with the laboratory for any specific instructions.
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 G6PC Gene Glycogen Storage Disease Type 1A 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.

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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.

  • ✓Individuals with symptoms suggestive of GSD Ia, such as severe hypoglycemia, enlarged liver (hepatomegaly), or poor growth.
  • ✓Family history of Glycogen Storage Disease Type 1A.
  • ✓Confirmation of diagnosis in individuals suspected of having GSD Ia.
  • ✓Genetic counseling for families affected by GSD Ia.
  • ✓Prenatal diagnosis for families with a known history of GSD Ia.
02

In plain language

What this test helps you understand

This test helps confirm or rule out a diagnosis of Glycogen Storage Disease Type 1A (GSD Ia) by identifying mutations in the G6PC gene. It can aid in understanding the underlying cause of symptoms related to glucose metabolism and glycogen storage.
The G6PC Gene Glycogen Storage Disease Type 1A NGS Genetic DNA Test is a diagnostic tool used to identify Glycogen Storage Disease Type 1A (GSD Ia), a rare inherited metabolic disorder. This condition affects the body's ability to process glucose, leading to the buildup of glycogen in the liver and kidneys. The test utilizes Next Generation Sequencing (NGS) technology to analyze the G6PC gene, which provides instructions for making an enzyme essential for glucose metabolism. Mutations in this gene are the cause of GSD Ia. Understanding your genetic predisposition can be crucial for managing health and planning for the future.
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 typically required for this blood test. However, confirm with the laboratory for any specific instructions.
SampleA blood sample is required for this test. Confirm specific collection requirements with the laboratory before booking.
MethodologyNext Generation Sequencing (NGS) is used to analyze the G6PC gene for mutations.
PrivacyYour sample and report are handled confidentially. Ask the team how your information is stored and shared.
This test analyzes the G6PC gene for common and some rare mutations associated with GSD Ia. It may not detect all possible mutations. A negative result does not completely rule out GSD Ia. 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

GSD Ia is a rare inherited metabolic disorder where the body cannot properly break down glycogen into glucose, leading to low blood sugar and glycogen buildup in organs like the liver and kidneys.
This test helps diagnose GSD Ia by identifying mutations in the G6PC gene. An accurate diagnosis is crucial for proper management, treatment, and genetic counseling.
Individuals with symptoms like low blood sugar, enlarged liver, or poor growth, or those with a family history of GSD Ia, should consider this test.
A genetic counselor or physician will interpret the results in the context of your clinical history. They will explain what the findings mean for your health and family.
Insurance coverage varies. Please check with your insurance provider regarding coverage for genetic testing.
The typical turnaround time is 3 to 4 weeks, but this can vary. Confirm the current timeframe 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.

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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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