Proactive Cancer Risk Test

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.

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. 1 in 20 people have a gene variation that increase their risk of developing cancer. Knowing whether or not there’s one in you or your family could be lifesaving.

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 of your data with anyone but you, the lab, and (with your express permission) your doctor. 

Each test comes with a consult with a Eugene genetic counsellor to discuss your results and any options you want to consider. If you’d like, we’ll also provide specialist referrals to support your ongoing care or forward your results to your GP or specialist.

1 in 20 people find out that they carry a variation in one of these 65 genes, which increases their lifetime risk of developing cancer.

Your prevention and screening plan depends on the gene variations found. Each variation that is screened for affects your risk differently and so the best approach to prevention and screening can be different.

Our genetic counsellor and physician team reviews your test results and your personal & family history to create tailored screening and prevention measures that you and your doctor can act on.

If needed, we’ll also provide specialist referrals to support your ongoing care.

This test focuses on genetic variants that are known to significantly increase the risk of developing a disease, ensuring you get clear and actionable insights. We may also share information on genetic variants that moderately affect your risk.

We don’t report on genetic variants with uncertain clinical impact, known as variants of uncertain significance (VUS), because they can’t be acted upon within a medical setting. Our goal is to provide you with information that empowers you to make informed decisions about your health.