Proactive cancer risk test

Understand your genetic risk of developing certain cancers.

At-home testing and online genetic counselling to help you make important health choices that are right for you.
$599 all inclusive
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Or from $40 a month

What is Eugene's proactive cancer risk test?

It's an at-home test that looks for genetic variations in 61 genes which can increase your risk of developing cancer.

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 on the test include —


Breast, ovarian, pancreatic, prostate cancer and melanoma.


Lynch Syndrome: bowel, ovarian and uterine cancer.


Breast, colorectal, endocrine, ovarian, and prostate cancer.

See a full list of genes

Relevant science things to know:

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.

Who is this test for?

Honestly, it’s for anyone who wants to be proactive about their health.

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.

When should you do it?

When you choose to have a proactive cancer risk test is completely personal.

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.

  • The test is not available to those under the age of 18.
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.

  • Caught early, some cancers have as high as 90% survival rate.
What do we test for?

Inherited gene variations that increase your risk of developing some of the most common types of cancer.

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.

See a full list of genes
Our honesty policy

The (not so) fine print.

What this test CAN DO:
  • Help people better understand their genetic risk of developing cancer.
  • Play an important role, along with your personal and family history, in creating your personal risk report and action plan.
  • Be the first step toward a tailored monitoring plan to enable early diagnosis of any cancer – to improve your chances of beating it.
  • Be the first step toward a tailored prevention plan to prevent a cancer from ever developing in the first place.
What this test CANNOT DO:
  • Diagnose you with cancer.
  • Tell you that you are certain to develop cancer.
  • Tell you that you are certain to never develop cancer.
  • Change your genetics in any way.
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Frequently Asked Questions

What is genetic counselling?


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.

If a gene variation is found that increases my risk, does that mean I will develop cancer?


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.

Could this test affect my ability to get insurance?


In some cases this test could impact your ability to get life or income protection insurance.

Not impacted—

  • Your ability to get health insurance
  • Your existing life and/or income protection cover. However, if you want to take out cover or change your existing policy, this test may have an impact.
  • Life and other insurances through super that are group policies and don't take into account personal medical history.
  • If your result doesn't identify a gene variant then your insurance shouldn't be impacted.

Could have an impact —

  • If you want to take out cover or change your existing policy, this test may have an impact.
  • On policies that do consider your medical history, like underwritten policies above certain coverage amounts (currently $500,000 for life insurance). If a gene variation that increases your risk of cancer is identified before you have taken out cover, you may be denied cover, or have to pay a higher premium or have policy exclusions.

For more information about how life and other insurance products may be impacted by genetic testing, visit the Financial Services Council or the Center for Genetics Education website.

How are my results used by my doctor in my ongoing care?


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.

How can I share results with my doctor?


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.

What's the turnaround time?


From the moment we receive your saliva sample, the turnaround time to get your results is 3 to 6 weeks.

Is there support to help me understand my results?


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.

Are my results and personal info protected?


As a healthcare company, we comply with the most stringent local and international 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.

I don't have a family history of cancer, is this still relevant for me?


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.

What happens to my sample once the test is complete?


Your saliva sample is destroyed after 60 days. In unusual cases when testing takes longer than 30 days, the specimen will be retained until the report is delivered.

More questions?

We’ve pulled together a few other things we think might help in this FAQ – if you have any more questions for us, just get in touch!
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