Health reports are already available via our lab partner, with app-based viewing for longevity, prevention, nutrition, fitness, medication response, ancestry, and family planning — with room to grow as science advances. App access is live and currently available through limited early access.
What you learn
Genetic insights organised into practical categories for long-term health, prevention, and personal planning.
Category 01
Healthy ageing, prevention, inflammation, recovery, and long-term resilience.
Category 02
Inherited markers that may influence cardiovascular risk and long-term prevention.
Category 03
How your genes may influence response to selected medicines, including metabolism and sensitivity.
Category 04
Metabolism, vitamin needs, caffeine sensitivity, food response, and diet-related traits.
Category 05
Endurance, strength, recovery, injury risk, and training response.
Category 06
Carrier status insights for inherited conditions that may matter for future family planning.
Category 07
Maternal, paternal, and broader heritage insights from your DNA.
Category 08
Selected traits linked to sleep patterns, stress response, and wellbeing.
How reports help
Use insights to support prevention and lifestyle choices, and to prepare conversations with healthcare professionals — not as a diagnosis.
Understand inherited risks that may be worth monitoring earlier or discussing with a professional.
Use genetic insights to guide diet, training, recovery, and long-term lifestyle choices.
See how your genes may influence response, metabolism, or sensitivity to selected medicines.
Review carrier status insights that may matter before or during family planning.
Report experience
What was analysed, what it means, and when to seek professional guidance — without leaving you guessing.
See which genes, variants, or evidence areas were included in the report.
A simple explanation of the result and what it may mean for your health.
Whether the finding is well established or still developing.
When a result should be reviewed with a doctor, pharmacist, or genetic counsellor.
See when updates become available — and keep reports connected to your data choices.
Inside the app
Your personal genome dashboard — view reports, track new insights, and manage privacy in one place.
Why 30x matters
Selected-marker tests check limited points. 30x whole genome sequencing builds a foundation for deeper reports and future reanalysis.
Selected points only — useful for ancestry and basic traits, but may miss important genetic variation.
Reads across most of your genome and creates a broader genomic record for supported analysis.
Mostly ancestry and a limited set of trait markers — less room for clinical-adjacent categories.
Supports longevity, heart health, medication, nutrition, fitness, family planning, and more.
Often a one-time snapshot — limited foundation when science and report libraries move forward.
Same stored genome, new insights as interpretation improves — still under your privacy controls.
Reports that evolve
You are not buying a static report. You are building a long-term health foundation as interpretation improves.
MyDNABank reports should be viewed as health insights and educational information unless reviewed through an appropriate clinical pathway. Actionable findings should be discussed with a qualified healthcare professional or genetic counsellor. We explain what each report does and does not mean, flag findings that may need professional review, and avoid fear-based reporting.