Fast, hassle-free patient referrals
Complete testing and counselling, no extra admin
Flexible, lab-agnostic integration
SOC 2 compliant data handling
Clinically actionable results support informed decisions
Every Eugene patient gets a clinical-grade lab report, a personalised counselling session, and a screening plan you can act on. Enter your details to see real sample reports for both low-risk and increased-risk results.
For clinicians
Genomic screening, integrated into your clinical practice.
Medical-grade testing for reproductive, inherited cancer, and heart disease risks. Every patient comes back with a personalised action plan, walked through one-on-one by a certified genetic counsellor and reviewed by a clinical geneticist.
40,000+
Australians screened
NPS 80+
Patient satisfaction
500+
Doctors actively referring
Two clinical categories.One platform.
Preventative Screening
Inherited risk for cancer, heart disease, and more
180+ clinically validated genes across three test options - Preventative Health, Cancer Risk, and Cardiac Risk - for asymptomatic patients. Recommendations for screening and medical management where risk is found.
Reproductive Carrier Screening
Family planning, coming soon
Help couples and individuals planning a family understand their chances of passing on inherited conditions. Three panel sizes from 3 to 780+ genes, with Medicare-funded support for couples at increased risk.
HGSA-certified genetic counsellors
NATA or CLIA accredited lab partners
Reviewed by clinical geneticists
SOC 2 Type 2 certified data handling
Why clinicians choose to bring Eugene in.
Eugene takes the parts of genetic testing that are hardest for a clinician to handle alone. We ensure both you and your patients have the right information at the right time to support informed decision making and integration of results into care plans.
01
Every patient gets an action plan
Personalised recommendations based on personal history, family history, and genetic results. You refer the patient; we return a plan you can use.
02
Genetic counselling, included
Every patient can have a one-on-one consult with a certified genetic counsellor who explains the result and walks through next steps. You don't need to be the genetics expert - we are.
03
Clinical geneticists in the loop
Every result is reviewed by a clinical geneticist in the relevant field - cancer, cardiac, or reproductive. You get an action-ready clinical summary, and we stay available for case discussion.
04
Built around your workflow
Referring takes a minute. Eugene handles kit, lab, counselling, and reporting. The only touchpoint after the order is the clinical summary letter that lands in your inbox.
Save time, improve patient care
Streamlined genetic testing
Give patients access to advanced genetic insights while Eugene handles the logistics, analysis, counselling, and compliance.
Features
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Fast, hassle-free patient referrals
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Complete testing and counselling, no extra admin
-
Flexible, lab-agnostic integration
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SOC 2 compliant data handling
Benefits
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Clinically actionable results support informed decisions
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Medicare rebated pathways for easier access
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Action plan for every patient, regardless of finding
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Seamless workflow integration
How it works
Five steps from referral to clinical summary.
4 to 6 weeks end to end. We handle everything between order and report.
1
Refer the patient
1-minute referral through your dedicated partner URL.
2
Patient collects sample
At-home saliva kit, prepaid return envelope.
3
Lab analysis
Accredited partner laboratories.
4
Patient counselling
Certified counsellor, one-on-one telehealth.
5
Summary to you
Action-ready clinical summary letter in your inbox.
What this looks like in practice.
Reproductive
Carrier couple identified pre-conception
A couple in their early 30s came in pre-conception. Both partners screened with our expanded carrier panel. Eugene identified them as a carrier couple for cystic fibrosis - a 1 in 4 chance of an affected child with each pregnancy. Their counsellor walked them through reproductive options. They chose IVF with preimplantation genetic testing and now have an unaffected child.
Preventative
Pathogenic SMAD9 variant found, no prior history
A patient in her late 30s. No personal or family history of cardiac disease. The Preventative Health Test identified a pathogenic variant in SMAD9, increasing her risk of pulmonary arterial hypertension. She and her children were referred to a cardiologist for monitoring. Without screening, she could have faced sudden cardiac death decades later.
See exactly what your patients receive.
Ready to bring genomic screening into your practice?
Refer a patient in a minute, or talk to our partnerships team about offering Eugene at your clinic.
