myDNA Comprehensive Health Report
$357.00
Comprehensive pharmacogenomic and nutrigenomic DNA test analysing 100+ genetic variants across drug metabolism, nutrient processing, fitness response, and disease predisposition. Provides personalised insights into how your body handles medications, caffeine, alcohol, vitamins, macronutrients, and exercise.
Description
What Is myDNA Comprehensive Health?
The myDNA Comprehensive Health Report is an Australian-developed DNA test that analyses over 100 genetic variants across multiple health domains — including pharmacogenomics (how you metabolise medications), nutrigenomics (how you process nutrients), fitness genomics, and disease risk. It is one of the most clinically actionable genetic panels available in Australia.
Unlike consumer ancestry-style tests, myDNA is designed for clinical use. Results are interpreted through the lens of evidence-based pharmacogenomic and nutrigenomic guidelines, providing Rohan with practical data to personalise your medication choices, supplement protocols, dietary strategy, and exercise programming.
What Does It Measure?
Pharmacogenomics (Drug Metabolism)
Analyses key cytochrome P450 enzymes (CYP2D6, CYP2C19, CYP2C9, CYP3A4, CYP1A2) and other drug-metabolising genes. These determine whether you are a poor, intermediate, normal, or ultra-rapid metaboliser of specific medications — including antidepressants, pain medications, cardiovascular drugs, proton pump inhibitors, and more.
Nutrigenomics (Nutrient Processing)
Genetic variants affecting how you absorb, transport, and utilise key nutrients — including folate (MTHFR), vitamin D (VDR, GC), vitamin B12, omega-3 fatty acids, iron, caffeine (CYP1A2), alcohol (ALDH2, ADH1B), and lactose tolerance. These insights directly inform dietary and supplementation decisions.
Fitness Genomics
Variants affecting muscle fibre composition (ACTN3), endurance capacity (ACE), injury risk, recovery speed, and optimal exercise type. Useful for patients looking to optimise their training or those who have struggled with exercise-related injuries.
Disease Predisposition
Genetic risk markers for conditions including cardiovascular disease, type 2 diabetes, coeliac disease, and other relevant health conditions. These are not diagnostic but help guide preventive strategies and monitoring.
Who Should Consider This Test?
This test is particularly valuable for patients experiencing:
• Adverse reactions or poor response to medications — especially antidepressants, pain medications, or PPIs
• Uncertainty about which supplements will actually work for their genetics
• Caffeine sensitivity, alcohol flushing, or unusual reactions to common substances
• Interest in a personalised nutrition and exercise strategy based on their DNA
• Family history of cardiovascular disease, diabetes, or coeliac disease
• Chronic health issues where a genetic contribution is suspected but not yet tested
• Anyone wanting a comprehensive genetic health baseline
Sample Collection
Sample type: Saliva sample
Collection method: Simple saliva collection into the provided tube — takes under 5 minutes
Fasting required: No food, drink, or gum for 30 minutes before collection
Medications: No restrictions — genetic results are not affected by current medications or supplements
Turnaround Time
Results are typically returned within 3-4 weeks from the date the laboratory receives your sample. Samples are processed in Australia by myDNA’s NATA-accredited laboratory.
What Happens After You Order
1. Kit dispatched — Your myDNA saliva collection kit is posted directly to your door with full instructions.
2. Collect at home — Follow the simple saliva collection protocol.
3. Post back — Mail the completed kit to the lab using the prepaid return envelope.
4. Results released to you — If you’re an existing patient, Rohan will go through the result with you at your next appointment. If you have your own practitioner, you’re welcome to order through Elemental Health and share the results with them directly.
Why Choose Elemental Health?
Rohan integrates pharmacogenomic and nutrigenomic data into everyday clinical practice — not as a standalone novelty test, but as a practical tool that directly informs treatment decisions. Every result is reviewed in the context of your full clinical picture, current medications, and health goals. Your consultation will include a clear, prioritised strategy covering medication adjustments (where appropriate), targeted supplementation, dietary personalisation, and exercise recommendations.
