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
Precision Prostate Cancer Screening: Moving From One-Size-Fits-All to Risk Stratified Prevention
Recent studies show that genomic risk modelling can refine prostate cancer screening by combining polygenic risk scores, family history, and genetic ancestry. This risk stratified approach enables more precise identification of individuals at higher risk while reducing unnecessary testing for lower-risk patients.
Defining Boundaries in Genomic Newborn Screening: Consent, Actionability, and Long‑Term Stewardship
Genomic sequencing in newborn screening can detect rare but treatable childhood conditions before symptoms appear, enabling timely interventions. By combining structured reporting with integrated genetic counselling, findings can be translated into actionable care. This approach helps ensure that early detection leads to meaningful outcomes while minimizing uncertainty or unnecessary surveillance.
From Eligibility Criteria to Preventive Insight: The Expanding Role of Population Genomics
A pilot population genomic screening program in Australia revealed that nearly 2% of young adults carry pathogenic variants missed by traditional guidelines. Structured interpretation, reporting, and counselling help ensure early, preventive care for at-risk individuals.

