At-home testing and online genetic counselling to help you make important health choices that are right for you.
$599 all inclusive
The test can help you determine if you have inherited a genetic risk for some of the more common types of cancer including — breast, ovarian, bowel and prostate cancer.
Some of the genes included on this test —
Cancer happens when cells grow and divide uncontrollably
These cancer cells grow at a faster rate than they die, which then causes a tumour to develop.
Sometimes we inherit gene variations that increase our risk of cancer
Even though all cancer is genetic, only some of us are born with a higher chance of developing it.
Cancer does not discriminate and can affect us all
Gene variations that increase cancer risk can be carried by people of any age, gender and ethnicity.
Know your risk so you can take action
Knowledge of your risk can open up access to preventative care and also influence the way you go about planning a family.
Important choices for you and your family
Your genetic risk can affect family members too. Help your loved ones understand your results and how their health could be impacted.
Better long-term health outcomes
Clarify any extra steps you can take that are beyond general health advice. Prevention and early diagnosis can improve long-term health outcomes.
Know more, know earlier
Understanding your risk can influence the way you plan a pregnancy, your lifestyle choices and your ability to access funded surveillance programs and risk reducing treatments
Early diagnosis saves lives
Knowing your genetic risk is the first step toward a tailored prevention & monitoring plan to help you catch cancer early – to improve your chances of beating it.
Your DNA is analysed in a CLIA and CAP certified laboratory for variations in 61 genes associated with some of the most common types of cancer — including breast, ovarian, pancreatic, prostate cancer and melanoma.
Send this to the people you trust to speak to about your health — whether that’s your partner, parent, doctor or friend.
Genetic counsellors guide people in making important decisions around how genetics influences their health. They are not doctors, but are genetic specialists that are trained to identify, explore and explain genetic risk. They can help you be practically and emotionally prepared to make empowered choices that feel right for you.
At no additional cost, connect with your Eugene genetic counsellor to discuss your test results. They can help you understand your results, answer any questions and help you learn more about what your results mean for you.
No. Genetics is only one part of the cancer risk puzzle. Having a gene variant in one of the genes included on our test will increase your chance of developing cancer, but not everyone who has a gene variation will get cancer in their lifetime.
There are many other factors that contribute to your risk, including environmental factors like exposure to the sun and lifestyle factors like smoking and exercise. If a gene variant is identified on our test, your results will include information about the specific gene variation you carry and how it influences your cancer risk so you can better understand your lifetime chance of developing that specific type cancer.
In some cases this test could impact your ability to get life or income protection insurance.
Could have an impact —
Your result will help you and your doctor determine any action strategies for prevention and early detection that might be appropriate for you.
You can learn more about that here.
Eugene’s proactive cancer risk test includes a personal clinical report that will have details about your results, that you can share with your doctor. The clinical report is available for you when you receive your results.
You can also speak with a Eugene genetic counsellor at no additional charge. Genetic counsellors can help you understand your results, consider next steps, and discuss how to share information with doctors and family.
From the moment we receive your saliva sample, the turnaround time to get your results are 3 to 6 weeks.
Absolutely! Each test comes with a post test genetic counselling session. Your Eugene genetic counsellors are all trained and have practiced across a number of specialties in addition to carrier screening and together with our consultant geneticists and widespread network of healthcare professionals, we make sure you’re always connected and supported.
As a healthcare company, we comply with the most stringent local and inernational privacy and security regulations. We take incredible care to use technical, process and physical safeguards to secure your personal information and protect it against misuse, loss or alteration.
Finally, Eugene doesn’t share any your data with anyone but you and (with your express permission) your doctor.
Yes. Even if you don’t have a family history you could still have a genetic risk that increases your own risk. Not everyone who carries an increased risk gene variant will develop cancer, so not every family will have a cancer history. So, while gene variations that increase cancer risk are rare, knowing whether or not there’s one in you or your family could be lifesaving.
Your saliva sample is destroyed after 30 days. In unusual cases when testing takes longer than 30 days, the specimen will be retained until the report is delivered.
We’ve pulled together other things we think might help in this FAQ – if you have any more questions for us, just get in touch!