myGeneticRisk - Intelligenetic

myGeneticRisk

The most common diseases do not discriminate – but being prepared is your choice.

Did you know that in Hungary, tens of thousands of deaths could be prevented each year through preventive measures? Genetic testing can increase the chances of detecting certain diseases at an early stage. Between 5–20% of cancers and around 30% of sudden cardiac deaths have an inherited genetic cause.

What if, with a single lifetime analysis, you could unlock the information hidden in your genes and turn uncertainty into a clear action plan?

myGeneticRisk can give you a lifelong health roadmap. Through our comprehensive genetic analysis, we identify inherited risks for cardiovascular diseases and cancers – the two most common causes of illness and death worldwide – enabling you and your doctor to take proactive steps.

Knowing your predisposition to these conditions allows fear and uncertainty to be replaced with a personalized prevention strategy, helping to prevent disease or detect it at an early, more treatable stage.

Instead of focusing on a single disease, we provide a fuller picture. Using state-of-the-art whole exome sequencing technology, we analyze 162 clinically relevant genes linked to actionable conditions – including those recommended for screening by the American College of Medical Genetics and Genomics (ACMG).

Who is myGeneticRisk for?

myGeneticRisk is not just a screening test – it is a strategic tool for those who want to take an active role in shaping their health. It is particularly relevant if any of the following apply to you:

Any healthy person who believes in prevention and proactively manages their health.

You don’t wait for symptoms – you take preventive steps to make the best possible health decisions.

As an athlete or active individual, you want to perform at your best.

You want to be sure there are no hidden cardiovascular risks in your genes that could undermine your performance or endanger your health.

You want to know your inherited cancer risk.

You want to replace uncertainty with knowledge – and receive a clear, evidence-based answer as to whether you carry an inherited cancer risk, and what you can do to protect yourself and your loved ones.

myGeneticRisk

The most common diseases do not discriminate – but being prepared is your choice.

What if, with a single lifetime analysis, you could unlock the information hidden in your genes and turn uncertainty into a clear action plan?

Who is myGeneticRisk for?

Any healthy person who believes in prevention and proactively manages their health.

You don’t wait for symptoms – you take preventive steps to make the best possible health decisions.

As an athlete or active individual, you want to perform at your best.

You want to be sure there are no hidden cardiovascular risks in your genes that could undermine your performance or endanger your health.

You want to know your inherited cancer risk.

Why is whole exome sequencing important?

Future-proof technology – your lifelong health data asset

myGeneticRisk is not a one-time snapshot – it is a lifetime investment in your future. We use the most advanced Whole Exome Sequencing (WES) technology, meaning we do not only analyze the 162 genes currently known to be relevant, but we record a large, significant portion of your entire genetic “library.”

The key advantage? As science advances and new genes are identified as important for health, your data can be reanalyzed – without the need for another sample. Your genetic information becomes more valuable over time.

Hidden risks are more common than you think

Between 5-20% of cancers are hereditary, the proportion varying depending on the type of cancer. Knowing this gives a chance for targeted screenings and effective prevention:

5–20%

Between 5–20% of cancers are hereditary, depending on the type. Knowing this risk can allow for targeted screening and effective prevention.

30%

Around 30% of sudden deaths are linked to unnoticed genetic abnormalities affecting the heart’s structure or rhythm. Identifying these in time can save lives.

5,4%

Research shows that more than 1 in 20 people (5.4%) carry a clinically relevant genetic variant (in ACMG-recommended genes) that can guide proactive health measures. Knowledge is power.

myGeneticRisk analyzes your risk for common genetic diseases. More than just a finding: A personalized health strategy if needed

myGeneticRisk is not just a lab report – it is a complete, expert-supported service that turns knowledge into a practical action plan when needed.

A comprehensive picture of the risk of common genetic diseases

Instead of focusing on a single disease, we provide a comprehensive picture. Using state-of-the-art technology, we analyze 162 clinically important genes. The test includes the most important genes associated with hereditary risk of cardiovascular disease and cancer, and complements the analysis with other diseases recommended for testing by the ACMG (American College of Medical Genetics and Genomics).

A lifetime, future-proof investment

Because your genetic makeup doesn't change, the test only needs to be done once. However, thanks to whole exome sequencing, your data becomes a future-proof health data asset that can be reanalyzed in the future as science advances - without having to take another sample.

Personal guidance – from knowledge to action

We do not leave you alone with your results. Pre- and post-test consultations with a clinical geneticist are an integral part of the service. Our experts help interpret your results and, if necessary, develop a personalized prevention plan. In the case of a positive result, we also provide guidance for targeted screening of at-risk family members, protecting your loved ones as well.

Your safety and long-term health are the focus of every element of the myGeneticRisk service. Detailed reports are usually available within 8 weeks.

Your personal advantage with myGeneticRisk – from knowledge to action

myGeneticRisk is more than a test – it is a comprehensive service dedicated to your long-term health and peace of mind. Genetic testing can significantly reduce the impact of hereditary cancers and heart disease.

A personalized prevention strategy

Instead of worrying in general terms, the test provides specific, scientifically based information about your risk for the most common hereditary cancers and cardiovascular diseases. This knowledge allows you and your doctor to develop a personalized prevention and screening plan, if necessary, giving you a chance to avoid the diseases or detect them at an early, more effectively treatable stage.

Expert support when it matters most

We understand that waiting for and interpreting genetic results can be emotionally challenging. That’s why we provide full professional guidance before and after the test. Our goal is not only to deliver results but to help you understand them and turn fear into an actionable plan.

A lifetime of expanding knowledge

Thanks to cutting-edge technology, you only need to take the test once. Your genetic data becomes a lifelong, secure data asset that can be reanalyzed in the future as science advances. This means your investment can become more valuable over time as new discoveries are made – all without having to take another sample.

Your path to conscious health – in 4 simple steps

myGeneticRisk is a complete service guiding you through every stage of the process, keeping it simple, transparent, and reassuring.

Step 1: Consultation and planning

It all begins with a conversation. You can book a free, no-obligation consultation with our clinical genetics expert. This is your chance to ask questions and assess whether the test is the right choice for you. We support you in making an informed decision.

Step 2: Simple sample collection

The analysis requires a quick, painless sample collection (typically a blood draw or saliva sample).

Step 3: Comprehensive laboratory analysis

Your sample is analyzed using state-of-the-art Whole Exome Sequencing (WES) technology. This in-depth analysis ensures the most accurate and comprehensive results. The full evaluation typically takes around 8 weeks.

Step 4: Results and, if needed, a personalized action plan

When your results are ready, you receive more than a report. In a personal consultation, our geneticist explains your results in clear, accessible language, helps you interpret them, and, if necessary, turns them into a specific, personalized prevention plan.

One investment, lifelong value

Test fee: 649,000 HUF

This fee covers the complete service: cutting-edge WES analysis of 162 genes, expert clinical genetics consultations at every stage, and the creation of a lifelong, reanalyzable health data asset.

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Frequently Asked Questions

Why does the myGeneticRisk test cost this much? How is it different from cheaper genetic tests?

myGeneticRisk is not just a test – it is a comprehensive, clinical-grade healthcare service. The price reflects:

The most advanced technology: We use Whole Exome Sequencing (WES) – the most comprehensive method available – to create a lifelong genetic data asset that can be reanalyzed in the future without needing a new sample.
Comprehensive analysis: We do not focus on just one or two diseases, but analyze 162 clinically important genes covering the most common hereditary cancer and cardiovascular risks.
Expert support: The price includes essential pre- and post-test consultations with a clinical geneticist. We don’t leave you alone with your results – we help turn them into a practical action plan.

By contrast, many cheaper tests on the market examine a much smaller number of genes and may not include any personalized medical consultation.

What happens if I get bad news? I’m worried about the possible results.

This is a completely understandable and common concern. One of the most important aspects of our service is that you are never left to face results on your own.

Our goal is not to deliver a “verdict,” but to create a personalized prevention plan. Our geneticist will help you interpret the results and turn this knowledge into a clear, proactive strategy so you and your doctor can take control of your health.

Knowledge – even if challenging – can replace uncertainty with power and direction.

Are my genetic data safe?

We are fully committed to protecting the security and confidentiality of your data. We strictly comply with the highest European and Hungarian data protection standards (GDPR).

Your genetic data is treated as strictly confidential medical information. It is stored securely and will never be sold or shared with any third party without your explicit consent.

How is this test different from prenatal genetic screening during pregnancy?

Prenatal genetic tests focus on the baby’s health during pregnancy and on detecting chromosomal abnormalities in the fetus.

myGeneticRisk, however, focuses on your own lifetime inherited health risks as an adult. The two tests serve completely different purposes: one supports a safe pregnancy, the other helps you manage your long-term health proactively.

Is the sample collection painful or complicated?

Not at all. The process is simple, quick, and painless – similar to a routine blood draw, or it can even be done using a saliva sample.

How long will it take to receive my results?

Whole Exome Sequencing is a highly thorough and complex laboratory process. From the time your sample is received, your detailed, fully evaluated report is usually ready within 8 weeks.