Your DNA holds the answers. We help you find them.
Advanced pharmacogenomics and genetic screening, helping patients and clinicians make better decisions, together.
Expert scientists
Qualified geneticists behind every report
SA-based laboratory
Local processing, faster results
Comprehensive testing
Tests covering every major genetic health area
Personalised medicine
Results built around your genetics, not averages
Why this matters
Your genetic profile is missing from almost every healthcare decision made about you.
Not because it isn’t relevant. Because until recently, reading it wasn’t practical. That’s changed. And the implications touch every area of your health.
Medication
Your genes determine how drugs work in your body
The same dose of the same drug can be toxic for one person and ineffective for another, based entirely on genetic metabolism type.
A poor metaboliser on a standard antidepressant dose may experience toxicity. An ultrarapid metaboliser gets no benefit at all.
Cancer Risk
Inherited variants don't announce themselves
Hereditary cancer mutations are silent until they aren’t. Knowing your status (and your family’s) changes what gets screened, when, and how aggressively.
BRCA variants significantly elevate lifetime breast and ovarian cancer risk. Most carriers don't know they carry them.
Gut health
Your microbiome shapes more than digestion
The bacteria in your gut influence inflammation, mood, metabolism, and immune function. Understanding your microbial profile explains patterns that blood tests don’t.
Dysbiosis (microbial imbalance) is linked to IBS, mood disorders, skin conditions, and metabolic dysfunction.
Nutrition
Generic dietary advice ignores your biology
How you absorb vitamins, process carbohydrates, respond to caffeine, and regulate weight is encoded in your DNA, not in a population average.
Two people on the same diet can have opposite outcomes. Your genes explain the difference.
99%
people carry a genetic variant affecting how they metabolise at least one common drug class.
80%
of chronic disease risk is influenced by lifestyle and environment, but your genetic baseline determines your starting point.
90%
of people with hereditary cancer mutations have no family history of cancer to alert them.
99%
people carry a genetic variant affecting how they metabolise at least one common drug class.
80%
of chronic disease risk is influenced by lifestyle and environment, but your genetic baseline determines your starting point.
90%
of people with hereditary cancer mutations have no family history of cancer to alert them.
Our tests
Find the right test for you.
Clinically graded tests covering pharmacogenomics, cancer genetics, microbiome, nutrition, and whole genome sequencing, each built to answer a precise question about your health.
Pharmacogenomics
PGx Live
The only pharmacogenomics test in South Africa with a lifelong clinical portal. One blood draw. Unlimited future value.
Best for: Patients on multiple medications or starting psychiatric treatment
Pharmacogenomics
PGx Static
Same clinical-grade pharmacogenomics analysis. One comprehensive report, delivered once.
Best for: First-time genetic testing for medication response
Gut Health
Microbiome test
A detailed map of your gut microbiome. 80+ genera, actionable dietary guidance, home collection kit.
Best for: Digestive issues, immune health, weight management
Nutrition
Nutrigenomics Comprehensive
12 categories, 31 genetic results, 130+ page report with an AI-generated meal plan. Your body's nutritional blueprint.
Best for: Optimising diet, fitness, and long-term wellness
Nutrition & Wellbeing
Nutrigenomics Wellbeing
150+ traits across nutrition, fertility, mood, and inflammation. The broad view of how your genes shape daily health.
Best for: Understanding genetic factors affecting daily wellbeing
Whole Genome
Whole Genome Sequencing
Your entire genome, sequenced. Includes ACMG secondary findings. The most comprehensive genetic picture available anywhere in the world.
Best for: Comprehensive genetic analysis and future-proofing
Cancer Genetics
Familial Mutation
Targeted confirmation of a known hereditary cancer variant. For families with an established index case. Fast, focused, definitive.
Best for: Family members of patients with confirmed genetic mutations
Cancer Genetics
Cancer Screening
BRCA Panel, Oncomine Precision, Oncomine Myeloid, DPYD, and custom panels. Comprehensive hereditary cancer risk assessment.
Best for: Family history of cancer or proactive risk assessment
How it works
From sample to result
01
Simple sample collection
Depending on the test, collection is either done at home, arranged through your doctor, or via a phlebotomist who comes to you. We handle the logistics.
02
Processed locally, quickly
Every sample is analysed in our South African laboratory. Results are available within 10 working days to 4 weeks depending on the test.
03
Results explained at every level
For clinical genetic tests - including pharmacogenomics and cancer panels - your referring clinician receives a full debrief from our geneticist and walks you through the findings. For direct-to-patient tests like microbiome and nutrigenomics, your report is delivered with clear, actionable guidance built in.
For Patients
Your genes. Your health decisions.
You don’t have to wait for a diagnosis, an adverse reaction, or years of guesswork. One test gives you the information your doctors have never had, permanently.
- Know how your body processes medication before you start
- Understand your hereditary cancer risk with clarity, not anxiety
- Personalise your nutrition based on what your DNA actually needs
- Expert support available at every stage. Through your clinician or directly with our team


For clinicians
Prescribe with the full picture.
PGx testing integrates directly into your clinical workflow. Results include actionable drug-gene interaction summaries, formatted for the consultation, not the research paper.
- PGx Live portal: patient results accessible at the point of care, forever
- CPIC and ClinPGx aligned - familiar clinical language
- Covers 80+ genes, 240+ medications across all major drug classes
- Referral pathway designed to fit your existing process
What People Say
Real results. Real lives.
PGx Live
“I’d been on three different antidepressants over four years. Within weeks of my PGx results, my psychiatrist adjusted my prescription and everything changed.”
Patient, Cape Town
PGx Live
“The clinical portal is genuinely useful. I’ve started referring patients before we even begin pharmacotherapy — it saves time and takes the trial out of prescribing.”
General practitioner, Johannesburg
Cancer Genetics
“My BRCA result gave my whole family the chance to act before anything happened. The counsellor made an overwhelming conversation feel completely manageable.”
Patient, Pretoria
Start Today
You only need to do this once. Your DNA doesn't change.
Order your test online. Sample collection is arranged around you. Receive a report that informs your healthcare decisions for the rest of your life.

