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Proactive Heart Health Test

This at-home genetic test screens 83 genes that increase your risk of developing heart disease to help guide your personalised prevention and early detection plan.

 Screens 83 cardiac risk genes
 Saliva sample collection
 Free genetic counselling included

Test Details

What’s included

At-home sample collection kit

DNA analysis in a certified laboratory

Doctor reviewed test results

30 min consult with a genetic counsellor

Questions?

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 heart disease, so not every family will have a history of heart disease.

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 30 minute consult with a Eugene genetic counsellor to discuss your results with you and customise a prevention and screening plan. If needed, we’ll also provide specialist referrals to support your ongoing care.

In addition, you can also access our free education tools, or take your results to your GP or specialist for follow ups.

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.

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.