Preventative Health Test

This test screens for inherited risks linked to cancer, heart conditions, cholesterol disorders, metabolic issues and other medically actionable health conditions. It includes 180+ clinically validated genes across cancer (65+), cardiovascular (85+) and other health risks (25+).

Your results will fall into one of two main categories:

No actionable findings — no inherited risk factors were found across the 180+ genes we tested. You'll still get personalised guidance based on your health and family history.

An inherited risk was found — you carry a genetic variant linked to a specific condition. Your genetic counsellor will explain what this means and what to do next.In some cases, your results may also include carrier information relevant to your health or family members. Your genetic counsellor will explain if this applies to you.

Every result comes with personalised prevention and screening guidance.

No. It means you carry an inherited risk factor, not a diagnosis.
Your genetic counsellor will explain what this means and what you can do next.

If an inherited risk is found, your report will outline clear, medically supported next steps. These may include:
• When to begin cancer or heart screening, and how often.
• Evidence-based changes shown to reduce cancer or heart risk for your specific gene finding.
• Information you can discuss with your doctor, such as cholesterol-lowering therapy for familial hypercholesterolaemia or chemoprevention options for certain cancer risks.
• Whether your genetic result affects future procedures, anaesthesia safety, or clotting risk.
• Which relatives may benefit from testing, based on standard inheritance patterns.

A genetic counsellor will walk you through your report and help you understand what each next step means for you.

You’ll receive an at-home saliva kit.

Your sample is processed at our international medical laboratory that is CLIA (Clinical Laboratory Improvement Amendments) and CAP (College of American Pathology) certified.

Results take about 4 to 6 weeks.

Yes. You’ll speak with a genetic counsellor who explains your results and helps you understand your next steps.

The test uses clinical-grade sequencing reviewed by genetic specialists.
Only pathogenic or likely pathogenic variants are reported, ensuring results are medically actionable and clinically relevant.

Your data is encrypted and stored securely with SOC 2 Type I and II protection. Results are private and never shared without your consent. Our laboratory is CLIA and CAP certified, meaning it meets rigorous national standards and is subject to regular independent inspections.

For most people, the answer is no — but it depends on the type of insurance.

Private health insurance is fully protected. Insurers cannot deny you cover or increase your premiums based on a genetic test result.


Life insurance and income protection are covered by an industry moratorium, which means you generally don't have to disclose your result — favourable or unfavourable — for new policies up to $500,000. Above that threshold, disclosure may be required.

The Australian government is currently finalising legislation expected to ban genetic discrimination in life insurance underwriting entirely.

Please speak to your genetic counsellor for guidance on this before you test.

This test is relevant if you're looking for:
• inherited cancer risk (BRCA, Lynch syndrome)
• inherited heart conditions (FH, cardiomyopathy, arrhythmias)
• longevity screening
• family history risk assessment