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.
| What's included | |||
| Total genes screened |
3 genes
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620+ genes
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780+ genes
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| Who is this test for? |
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| Reproductive risk |
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| Individual carrier result |
Female only
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No individual carrier result
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| Medicare rebate |
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Partial rebate
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| Genetic counselling support |
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| Express return shipping |
$19.99
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Free
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Free
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| Results turnaround time |
Within 4 weeks
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Within 6-8 weeks
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Within 4 weeks
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What our community is saying
Millie
"The testing process is quick; it takes 3-6 weeks from the day they receive your sample to get the results back and schedule your appointment with a genetic counsellor to learn about your results and have an opportunity to ask any questions.
We did a Eugene test because we knew it would be the quickest way to get some reassurance before planning our next round of IVF and for our future."
Jamie
“Getting the results was an amazing experience as not only did it, give myself and my wife, a great sense of peace , but it was also really helpful to go through it with our OB. I would recommend the service to anyone who’s trying to have children. They really care about your experience and giving you the right information away that you can understand.”
Jasmine
"From the moment I reached out for a genetic screening for my partner and I, Eugene ensured that the entire process was smooth and easy to navigate. As someone who lives in a remote area, accessing such services can be challenging, but Eugene made it effortless through their excellent online communication platform."
Aliza
“Carrier screening is so simple Eugene sends you a testing kit, you & your partner do a saliva sample, and sent it back. The DNA from saliva is analysed. You then meet with a genetic counsellor who runs through both of your results, what it means if there are any risks and the next steps.”
Sarah
Very easy to use. From shipping straight to my door, saliva sample & prepaid return shipping, the longest part was waiting for the results (which only took 2-3 weeks). For the peace of mind, I definitely recommend this to anyone wanting to fall pregnant. So much so, I just ordered the expanded carrier screening kit.
Natashjja
"From ordering to the genetic counselling itself, 10/10! Everyone in the Eugene team is lovely, knowledgeable, and genuinely wants to make the experience a great one. It’s still wild to me that such a simple test can tell us so much, go science!"
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
How to refer a Patient for Genetic Testing at Eugene
At Eugene, our clinician-led team ensure that your patients have access to expert genetic counselling at every point of their journey. Results are delivered with clarity and compassion, supporting actionable insights and clear pathways. Referring your patients is straightforward and takes less than 60 seconds. Simply head to eugenelabs.com/pages/refer-a-patient, complete the short form with your patient’s details, and we’ll take care of the rest. Remember you can refer patients for both preventative and reproductive genetic testing, depending on their personal needs. Preventive Health For proactive screening, you can refer patients for: Proactive Cancer Screening Proactive Heart Disease Screening Preventative health screening, which screens for both cardiac and cancer-risk genes These tests help patients understand their inherited risk and make informed decisions about prevention, early detection, and management. Reproductive Carrier Screening Eugene offers three carrier screening options, tailored to different patient needs and life stages: Core Carrier Screening: This is a 3-gene panel which screens for: Cystic Fibrosis (CFTR) Spinal Muscular Atrophy (SMN1) and Fragile X Syndrome (FMR1) This test is covered by Medicare. In this test, we first screen females, which takes 4 weeks. If they are found to be carriers of cystic fibrosis or spinal muscular atrophy, then we provide carrier screening for their male partners to clarify their reproductive risk as a couple. Testing the female and male takes a total of 8 weeks. 2. Couples Carrier Screening (screening for 620 genes) This option screens for over 620 genes and is reported as a combined risk between a male and female. This test does NOT tell patients about their individual carrier status. Instead, their results are compared and they receive a low or increased risk result. The test takes about 8 weeks. This test is suitable for couples who are eligible for medicare, and are bringing an egg and sperm to the table. This option is not ideal for individuals testing alone, using a donor, or wanting their individual carrier status. 3. Comprehensive Carrier Screening Our most advanced option, which screens for 787 conditions, including: The three core conditions, Tay-Sachs Muscular Dystrophies Thalassaemia and hundreds more … It's particularly beneficial for patients from diverse ethnic backgrounds, rainbow families, patients interested in their individual carrier status, and those who want the most thorough option. Not sure which test is right for your patient? No problem. Our team guides each patient through their options, and all patients are offered a free consultation with a genetic counsellor before proceeding with testing. Once you’ve submitted the referral, we’ll be in touch with your patient directly and provide everything they need to get started! Results & reports All results are based on current evidence, focusing on pathogenic variants and management guidelines. Clinically actionable results only are reported. Therefore, there is no reporting on variants of unknown significance. Test results and reports are seamlessly integrated into clinical systems (Genie?), making referrals easy and fitting smoothly into your workflow. Please don’t hesitate to get in touch with any questions or queries you may have 😃 at hello@eugenelabs.com
What do my genetic results mean for me and my family?
Genetic testing provides valuable insights into your health, helping you understand your risks for certain conditions like cancer and heart disease. But what happens if your results show an increased risk? And what should you do next? Let’s break it down. An increased risk is not a diagnosis If your genetic test results indicate an increased risk for a condition, it doesn’t mean you have the disease- it simply means you may have a higher chance of developing it. Your risk level is determined by looking at your specific genetic variant, your personal and family medical history, and information about the condition itself. With this knowledge, you have an opportunity to take proactive steps. Clinical guidelines can help guide decisions about: Genetic testing provides valuable insights into your health, helping you understand your risks for certain conditions like cancer and heart disease. But what happens if your results show an increased risk? And what should you do next? Let’s break it down. What can I do with my results? Increased screenings – More frequent check-ups can help catch potential health issues early. Lifestyle changes – Adjustments in diet, exercise, or other habits may reduce your risk. Specialist care – We may refer you to a cardiologist, a familial cancer centre, or another expert. Should I share this information with my family? Since genetic conditions can sometimes run in families, your test results have implications for your relatives as well. Sharing this information can help them decide whether they should also consider genetic testing or take preventive steps for their own health. Deciding to share your results is a personal choice, but if you do, resources are available to help. At your results appointment, we can provide tools like family letters to make these conversations easier. Knowledge, power and prevention. While an increased risk may feel overwhelming at first, it’s important to remember that knowledge empowers you to take action. Your results don’t define your future- they give you the opportunity to make informed choices that could positively impact your long-term health. If you have questions or need support in understanding your results, book a free consultation with a Genetic Counsellor today. Together, we can create a plan that’s right for you.
Heart Health Inequality: Putting Women’s Hearts first
At Eugene, we are proud to support women daily as they navigate their reproductive health and their broader preventative health journey. Did you know? 20 Australian women die of heart failure each day, yet women are less likely to receive treatment for chest pain in hospital. [Heart Foundation] Although women and men have similar rates of heart failure, women are more than 35% less likely to participate in cardiac rehabilitation programs. [Wiley Online Library] A 2021 Australian study found that men are twice as likely as women to be diagnosed with hypertrophic cardiomyopathy, potentially because men are more likely to undergo echocardiograms. [ScienceDirect] There is a significant gap in research, randomised clinical trials and clinical treatment for women with cardiac failure, when compared to men (reference). This gap exists because much of the historical research focused on caucasian males, leading to a significant disparity in how we understand and diagnose heart conditions in women. Women are often told to watch for classic heart attack symptoms—like chest pain—when, in reality, their symptoms may present very differently. Here’s what to look out for: Heart attack symptoms in Women: Uncomfortable pressure, squeezing, or fullness in the chest, but not always severe or the most prominent symptom Pain in the back, neck, jaw, or stomach—this pain can be sudden or gradual and may come and go Shortness of breath with or without chest discomfort Nausea or vomiting Extreme fatigue, which can occur days or even weeks before the attack Lightheadedness or dizziness Cold sweats Indigestion or a feeling of heartburn Upper back pressure, which might feel like a squeezing or fullness Why knowing our genetic risk matters: Preventative health starts with your genes. With just a simple at-home saliva test, Eugene’s Preventative Health Test screens 167 genes to help create a personalised prevention and early detection plan for conditions like cancer and heart disease. The test includes: 65 genes associated with increased cancer risk, including breast, bowel, skin, and prostate cancers. 83 genes that increase your risk of common types of heart disease, including high cholesterol, high blood pressure, and conditions that could lead to heart attack and stroke. 19 additional health risk genes, covering conditions such as dystonia and hemochromatosis. Free genetic counselling before and after the test. Personalised action plan to guide proactive healthcare choices with your GP. How knowing your genetic risk empowers you: When you understand your genetic risk, you gain powerful insights into your health that allow you to advocate confidently for yourself with your medical team. Knowing your risk for conditions like heart disease and cancer helps you: Ask the right questions: Bring informed questions to your appointments and engage meaningfully with your healthcare providers. Build the right team: Find specialists who understand your genetic profile and can tailor your care accordingly. Proactively manage your health: Take preventative steps and access early detection strategies that could make a critical difference. Navigate the healthcare system with confidence: You’ll feel empowered to push for tests, screenings, and referrals when needed. Because when it comes to your health, knowledge is power—and you deserve nothing less. References: https://www.heartfoundation.org.au/your-heart/heart-conditions-in-women https://onlinelibrary.wiley.com/doi/full/10.1002/ejhf.3284 https://www.sciencedirect.com/science/article/pii/S1443950623044207
