Life-changing genetic insights for growing families and proactive health decisions
Australia’s leading at-home genomic healthcare service, offering inclusive, actionable genetic testing and counselling for reproductive and preventative health. Medicare available.
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Seamless genetic care, tailored to your needs
Plan for pregnancy, prioritise health, or integrate genetic services into your practice. Our at-home testing and expert genetic counselling make it easy to make proactive decisions—on your terms.
How testing works
On demand - simple, at-home testing and counselling
1. Order your test
Order online and delivered to your door
2. Share your story
Help us to make testing meaningful to you and your goals
3. Provide your sample
Simply swab and return your kit via prepaid package
4. Get your results
Free telehealth consult with an accredited genetic counsellor
Compare genetic tests
Explore genetic testing options tailored to your needs.
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| Reproductive risk |
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| Individual carrier result |
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| Medicare rebate |
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| Genetic counselling support |
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| Free express return shipping |
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Our purpose is to empower every person to act on this knowledge.
We provide inclusive, accessible genetic testing that empowers individuals and healthcare providers to make confident decisions. We are committed to human-centred care, innovation, and actionable health insights.
Empowering better health, together
25,000+
People gaining clarity and confidence in their health
500+
Doctors recommending Eugene to provide informed care
90%+
Patient satisfaction, with ongoing support at every step
Latest Insights and Updates
Explore our latest articles on genetic testing and health
Genetic discrimination by life insurers soon to be banned: Implications for Healthcare
Australia’s new legislation banning genetic discrimination by life insurers removes a long-standing barrier to genetic testing and preventive care. By separating clinical insight from insurance risk, the reform supports earlier screening, informed decision-making, and better health outcomes. For healthcare providers, it enables more confident, patient-centred integration of genetics into everyday care pathways.
BabyScreen+ : How Genomic Newborn Screening is Shaping Prevention-Focused Paediatric Care
The BabyScreen+ study shows how genomic newborn screening can extend standard programs to detect actionable conditions that may otherwise be missed. When supported by genetic counselling and scalable digital models, early genomic insight enables timely intervention, personalised care planning, and a shift toward prevention-focused paediatric care.
Sperm Donor with TP53 Mutation Fathers Nearly 200 Children: Implications for Reproductive and Fertility Care
Recent reporting of a sperm donor unknowingly carrying a rare TP53 mutation linked to Li-Fraumeni syndrome highlights the limits of genetic screening in donor conception. While testing reduces risk, it cannot eliminate it entirely- particularly for rare variants. This case reinforces the importance of genetic counselling, proactive risk management, and clear governance, including adherence to Australian donor limits and legislation, to support informed decision-making and protect the long-term wellbeing of donor-conceived families.

