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Our Tests
Preventative Health Test with Longev
The Preventative Health Test screens 167 genes that could increase your risk of developing certain cancers, heart disease & other health risks to help create a personalised prevention and early detection plan.
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Screens 167 genes: 65 cancer-risk genes 83 heart disease genes 19 additional health-risk genes |
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Simple at-home saliva test |
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Free genetic counselling before & after test |
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Personalised action plan |
Sample collection in clinic
No doctor referral needed
Results in 4-6 weeks
What genes are screened?
This bundle includes everything in our Proactive Cancer Risk test and Heart Health Test, plus extra health risk genes:
- 65 genes associated with increased cancer risk, including breast, bowel, skin & prostate, could also impact your child’s health.
- 83 genes that increase your risk of some of the most common types of heart disease including high cholesterol, high blood pressure & conditions that could lead to heart attack & stroke.
- 19 additional health risk genes including dystonia and hemochromatosis
What can I do with my preventative health test results?
Information about your genetic risk is simply the first step to action. We create a tailored action plan for you to prevent or reduce your risk of developing cancer & heart disease:
- Understand what lifestyle changes can help prevent cancer and heart disease
- Get access to risk-reducing medications
- In some cases, consider preventive surgery.
- Be prepared for future surgeries or c-sections by understanding any risks of clotting disorders or adverse responses to anaesthesia
- Identify more common heath risks like markers that predict an increased chance of clotting disorders or adverse responses to anaesthesia
About the lab
Your sample is processed at Invitae, an international medical laboratory that is CLIA (Clinical Laboratory Improvement Amendments) and CAP (College of American Pathology) certified.
This means they meet high standards to obtain national certifications and submit themselves to regular inspections.
What's included
At-home sample collection kit
DNA analysis in a certified laboratory
Doctor reviewed test results
A consult with a genetic counsellor
As featured in
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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.
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From the moment we receive your saliva sample, the turnaround time to get your results are 3 to 6 weeks.
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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 or heart disease, so not every family will have the family history. 1 in 7 people have a gene variation that increase their risk of developing cancer or heart disease. Knowing whether or not you have a gene variation could be lifesaving for you and your family.
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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.
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Your prevention and screening plan depends on the gene variations found. Each variation 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.
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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.