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
Whole-Genome Embryo Screening: What the Science Can Do and What It Has Not Yet Proven
Whole-genome embryo screening can predict polygenic disease risk across 12 conditions with high accuracy. But does technical capability translate into clinical utility? This post examines what the evidence shows, where it becomes more cautious, and what the scientific consensus means for clinicians supporting patients through IVF.
Familial Hypercholesterolemia: Why Current Screening Guidelines Are Missing Most Cases
Familial hypercholesterolemia affects approximately 1 in 200 people, is highly treatable, and passes silently through families for generations. A new study of more than 84,000 participants found that standard clinical criteria identified fewer than one in three confirmed cases. Here is what that means for cardiovascular risk assessment.
The Clinician's Role in Genomic Medicine: Why Trust Is the Foundation
As genomic testing moves into routine care across reproductive health, cardiovascular risk, and cancer prevention, a new systematic review makes one thing clear: patients look to their clinician first. How that conversation goes determines whether testing leads to meaningful health outcomes or confusion.

