Your genome already holds the answers. We make them clear and actionable.
Proactive Health Screening with backed by clinical guidelines.
A gene panel tailored to your ancestry.
Inherited conditions differ in how common they are across populations. That's why we offer panels with additional genes tailored to different population groups, so the conditions we screen for are relevant to your background. Select your option when you order.
The reference data used to interpret genetic tests still under-represents many populations outside Europe. Closing that gap is part of our mission.
Everything you need. In one box.
Clinical-grade genetic tests you can take at home, with expert genetic counselling included when it matters. For the health-conscious individual who wants answers before symptoms arise, our genetic screening tests offer a window into your future health.
- ✓Clear results and next steps
- ✓Tests designed on American College of Medical Genetics and Genomics guidelines
- ✓European lab
- ✓Privacy protection
Choose the screen that fits you.
Chat with TaraTrusted results, backed by science.
Proactive health screening, powered by an ISO 15189 and CAP accredited European clinical laboratory.
Assay maintains zero false-positive rates for single-nucleotide variants and small insertions/deletions
In validation testing, the method detected 99.57% of known single-letter DNA changes.
More than 99% of the DNA letters in the tested genes are each read over 20 times.
On average, each DNA letter is read 136 times.
Each test can find missing pieces of DNA as small as one exon, a single segment of a gene.
How It Works
From order to answers — seven steps, one hand to hold. A transparent end-to-end flow with expert human support built in.
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01Order
Order your test
Select your test through our secure online platform.
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02Educate
Pre-test education
Chat to Tara to learn more about your test and complete a medical history form.
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03Kit
Receive your kit
A collection kit is dispatched to your door, including all necessary components and instructions.
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04Swab
Simple cheek swab
Collect your DNA sample easily at home.
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05Return
Return your sample
Send your kit back to us in the prepaid return package.
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06Report
Secure digital reporting
If nothing shows up, a clear clinical report is delivered through our secure portal — ultimate peace of mind.
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07Guidance
Expert guidance & referral
A genetic counsellor guides you through significant findings and next steps.
From order to answers.
Seven steps, one hand to hold — with expert human support built in.
- Step 01Order your testSelect your test through our secure online platform. No referral needed for most tests.
- Step 02Pre-test educationComplete an interactive session with Tara to ensure you are confident and informed.
- Step 03Receive your kitA collection kit is dispatched to your door, including all necessary components and instructions.
- Step 04Simple cheek swabCollect your DNA sample easily at home — a few minutes, no appointment needed.
- Step 05Return your sampleSend your kit back to us in the prepaid return package.
- Step 06Secure digital reportingIf nothing shows up on your test, a clear clinical report is delivered through our secure portal, giving you ultimate peace of mind.
- Step 07Expert guidance & referralIf important findings are identified, our Genetic Counsellors guide you through with a 1-on-1 session, personalised action plan, specialist referrals, and emotional support.
Your questions,answered clearly.
Proactive genetic health testing analyses your DNA to identify variants linked to hereditary conditions — before symptoms appear. It screens for predispositions to hereditary cancers, cardiovascular disease, metabolic disorders, and more, so you can take early, informed action.
- Consumer tests. Sometimes called recreational tests, these usually check a limited number of known DNA variants. They are not designed to guide medical decisions.
- Clinical tests, like ours. These read the tested genes in detail, are performed in accredited clinical laboratories, and are interpreted by qualified genetics professionals. Results come with genetic counselling, so you and your doctor can use them to inform health and family planning decisions.
Our screening tests examine variants associated with many hereditary cancers such as breast and ovarian cancer (BRCA1/BRCA2), Lynch syndrome, hereditary cardiovascular disease, familial hypercholesterolaemia, metabolic disorders, and neurodegenerative conditions — all based on evidence-based clinical guidelines. Chat to Tara to discover more about each of our tests.
A qualified genetic counsellor will explain your results in plain language and provide a personalised, evidence-based report covering clinical and lifestyle recommendations, plus recommendations for specialist services where needed. You are never left to interpret your results alone.
How our tests are run. All our tests use clinical-grade sequencing in accredited laboratories. We report only variants classified as pathogenic or likely pathogenic, meaning known or likely to cause disease, under the international ACMG/AMP guidelines.
What a test can’t do. No genetic test is 100% accurate. Detection rates can also vary with ancestry, because some populations remain under-represented in the reference databases used to interpret results.
Options for your background. Inherited conditions differ in how common they are across populations, so we offer ancestry-specific options across our screening tests. These tailor the gene list to conditions relevant to your ancestral background.
- Your DNA data. Your test is processed by one of our laboratory partners, in Europe or Australia depending on the test you order. The laboratory stores your raw DNA data under the privacy laws that apply in that location.
- Your personal information and results. Genotype Health stores these in Australia, in line with Australian privacy law.
- Your access. You can ask to see your data at any time. See our privacy policy for details.
