Genetic Testing
CALR3 Gene Cardiomyopathy Familial Hypertrophic Type 19 Genetic Test
Genetic test to identify mutations in the CALR3 gene associated with Familial Hypertrophic Cardiomyopathy (HCM). Helps in understanding genetic risk for this heart condition.
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.
At a glance
Plan your test
- Sample
- Blood sample (collected in an appropriate tube), Extracted DNA, or One drop of blood on an FTA card.
- Results
- 3 to 4 Weeks. Confirm with the laboratory before booking.
- Preparation
- A clinical history of the patient is required. A genetic counseling session to draw a pedigree chart of affected family members is recommended before testing.
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 CALR3 Gene Cardiomyopathy Familial Hypertrophic Type 19 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.
Providers & schemes we can help you check
Government & public schemes
Eligibility and benefits follow the current rules of the Social Health Authority (SHA) and applicable government programmes.
Private insurers & employer schemes
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.
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 Hypertrophic Cardiomyopathy (HCM)
- ✓Unexplained heart failure
- ✓Symptoms suggestive of HCM (e.g., shortness of breath, chest pain, palpitations, fainting)
- ✓Personal history of HCM
- ✓Risk assessment for family members of HCM patients
- ✓Genetic counseling for cardiovascular risk
In plain language
What this test helps you understand
This test specifically looks for mutations in the CALR3 gene. By analyzing your genetic material, the test can provide insights into your likelihood of developing HCM.
Individuals with a family history of HCM, unexplained heart failure, or symptoms like shortness of breath, chest pain during exertion, palpitations, fainting, or dizziness may benefit from this test. A family history of cardiovascular diseases, especially HCM, is a key consideration.
Taking this test can lead to early detection of genetic predispositions to HCM, enabling informed decisions about lifestyle and treatment. It can also help guide family members about their potential risk and improve overall cardiovascular health management.
Results will indicate the presence or absence of mutations in the CALR3 gene. Discussing your results with a healthcare provider or genetic counselor is recommended to understand the implications and develop a personalized management plan.
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 →A simple process
What happens next?
You do not have to navigate the test alone. We help you move from question to next step.
Speak with us
We check the test and answer your questions before collection.
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.
Understand your report
A counselor helps you understand the result and the next steps.
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 →Read your report
What common result terms mean
Questions people ask
Frequently asked questions
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.
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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