myGenome - Intelligenetic
myGenome
The genetic foundation for a long and healthy life (Longevity)
Discover your genetic map for informed, long-term health preservation
myGenome is Intelligenetic’s most comprehensive genetic prevention test, developed for healthy individuals who wish to proactively care for their current and future health and are committed to a long, active, and healthy life (Longevity). This test is not merely a snapshot—it provides a lifelong genetic resource that forms the basis for your personalized Longevity strategy.
Why is myGenome the starting point for a Longevity strategy?
Modern medicine increasingly focuses on prevention and personalized solutions, especially to achieve healthy aging and long life expectancy. By sequencing your entire genome, myGenome offers deep insight into your unique genetic makeup, revealing predispositions and risks that may affect your health and lifespan.
Identify your genetic predispositions to the most common chronic diseases, including cardiovascular conditions and cancer risks. This knowledge empowers you to take targeted preventive measures and, together with your physician, develop a personalized health plan.
Genetic insights can help you optimize your diet, exercise routines, and other lifestyle factors to support healthy aging.
Carrier screening enables you to make responsible decisions about your family’s future.
Learn how your body responds to over 250 medications, reducing side effect risks and maximizing treatment effectiveness.
The data obtained from myGenome serves as your genetic “user manual.” As science advances, this information can be reinterpreted in light of the latest research, continuously supporting your journey toward a healthy, long life.
Why is whole genome sequencing important?
Think of your genetic code as a blueprint for your body. While exome sequencing offers a glimpse into the "parts list" (about 2% of your DNA), myGenome provides a view of the entire library (the "master blueprint") — complete with "parts," "millimeter-precise assembly instructions," and "rules of thumb.”
But why is this remaining 98% so vital to a long, healthy life? Because it's where the "master switches" that control your vitality and performance are located. These switches determine how you use nutrients, respond to exercise, metabolize drugs, and keep your body balanced over decades. That's the knowledge that exome scanning does not have.
Whole genome sequencing not only offers a more complete picture but also provides a resource you can revisit over time.
17%
17% of people carry genetic variants that increase disease risk.¹
20%
Up to 20% of certain cancers are linked to hereditary factors.²
20%
About 20% of sudden cardiac deaths are due to genetic disorders.³
5%
5% of patients are hospitalized due to adverse drug reactions.⁴
86%
86% of people unknowingly carry a monogenic disease that can be passed on to their children if their partner is also a carrier.⁵
6%
6% of the population has an increased risk of hereditary thrombosis.⁶
¹ Hou YC et al. Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging. Proc Natl Acad Sci U S A 2020 Feb 11;117(6):3053-3062.
² seom.org – Genetic Counseling Information
³ Orland KM et al. Molecular Autopsy for Sudden Cardiac Death: Current State and Considerations. Curr Genet Med Rep 2019;7:145–152.
⁴ Bouvy JC et al. Epidemiology of Adverse Drug Reactions in Europe. Drug Saf 2015;38:437–453.
⁵ Hou YC et al., ibid.
⁶ MacCallum P, et al. Diagnosis and management of heritable thrombophilias. BMJ 2014;349:g4387.
Detailed description of the myGenome service
myGenome is a whole genome sequencing and interpretation service focusing on disease prevention and health optimization. The test is performed from a simple saliva or blood sample. The entire genome is sequenced (Whole Genome Sequencing), and a comprehensive report is prepared. Every test must be ordered by a physician and includes both pre-test and post-test genetic counseling. The process, from sample arrival at the laboratory to analysis and report generation, takes approximately 12–14 weeks.
Technical Information
Genome sequencing with Illumina Nova Seq 6000 platform with an average depth of 30X (the gold standard for genome sequencing). Analytical sensitivity is 99% for SNVs* and 97.6% for small insertions/deletions (6 bases). Analysis and classification of variants based on internal and external databases (ClinVar and HGMD**). Version management by a dedicated team of experts with proprietary software developed for detailed version classification.
What does myGenome include?
The report contains actionable information in the following categories, always accompanied by genetic counseling before and after testing:
+650
Interpretation of genes associated with modifiable health-related conditions.
+225
Analysis of over 200 conditions that can be passed on to children.
+250
Analysis of metabolism for more than 250 medications.
+15
Conditions influenced by both genetic and environmental risk factors.
+50
Personal characteristics influenced by both genes and environment.
∞
DNA variant analysis to determine ancestral background.
Which conditions are analyzed?
The test pays particular attention to cardiovascular diseases and cancer risks. The analysis includes:
Cancer predispositions
Blood clotting disorders
Cardiovascular diseases
Organ health
Carrier screening
Endocrine and metabolic disorders
Neurological disorders
Mitochondrial diseases
We evaluate information recommended by leading genetic societies and focus on conditions that are preventable or better managed through early detection.
Contents of the myGenome Report – Your Personal Guide to Longevity
We will prepare a comprehensive report in English. The report will contain useful information in the following categories, which we can discuss during pre- and post-test genetic counseling:
Clinical Outcomes
Interpretation of genes associated with modifiable conditions that affect an individual's health (analysis of 566 genes) that are associated with more than 650 conditions that can have a significant impact on a patient's health. Knowledge of these is key for early detection and the development of preventive strategies.
Pharmacogenomics
Investigating the metabolism of over 250 drugs by studying genes related to metabolism, secondary targets and transporters. This contributes to safer and more effective drug therapies in the long term.
Carrier Status
Analysis of over 200 conditions that can be passed on to children and for which the patient may be an asymptomatic carrier.
Ancestry
Analysis of DNA variants to determine ancestral background.
Multifactorial Diseases
These are complex conditions in which both genetic and environmental risk factors play a role. Understanding these risks helps to plan targeted lifestyle changes.
Genetic Traits
Individual characteristics influenced by genes and environment, which can affect, for example, nutrient processing or athletic performance. The test pays particular attention to cardiovascular disease and cancer risk, which have a significant impact on lifespan and quality of life.
The test pays special attention to cardiovascular disease and cancer risk, which have a significant impact on lifespan and quality of life.
myGenome Advantages – Why Choose This Test for Your Longevity Goals?
Lifetime Value
A single sequencing is sufficient for the data used in the analysis. As scientific knowledge advances, your data can be reanalysed repeatedly for updated insights—making it a lifelong health resource. This dynamic approach ensures you always have access to the most current information about your health.
Modifiable Diseases
Targets early detection and better management of diseases selected by the Personal Genome Project and Harvard Medical School, enabling you to take proactive steps toward a healthier future.
Clinical Utility
The test has clinical utility that can be used by professionals in the provision of healthcare services and their personalization, especially with regard to long-term health maintenance strategies.
You don't just get a find, you get a team of experts
Expert Variant Interpretation
Our geneticists interpret variants using the latest scientific evidence, drawing on public, private, and Veritas’s proprietary databases.
Detailed Report
Comprehensive, English-language report with clear, easy-to-understand information.
Genetic Counselling
Genetic counseling before and after the test in Hungarian, with the support of specialists and patients. During the counseling, you can discuss how the results can be integrated into your personal Longevity plan.
Data alone is just noise. We give it meaning. myGenome doesn't end with the discovery, but it begins with a conversation about your future.
Target Audience
The myGenome test is intended for healthy adults who proactively manage their health, are interested in disease prevention, and want to build a conscious foundation for a long and healthy life. For minors, we recommend the myNewborn genetic screening test.
Take a Step Toward a Long and Healthy Life
The myGenome test offers a unique opportunity to gain deep insights into your genetic heritage and use this knowledge to actively shape your health and support your longevity.
Price: 1,170,000 HUF
Request a personalised consultation to explore the longevity potential of myGenome!
Appointments: Online or by phone at +36 1 700 1303
Frequently Asked Questions
myGenome is a genetic sequencing test performed from a simple saliva or blood sample. We sequence the entire genome (Whole Genome Sequencing) and provide a complete report on the results. All tests must be ordered by a physician and include both pre- and post-test genetic counselling.
The process takes approximately 12–14 weeks from the sample’s arrival at the laboratory to analysis and reporting. Timelines may vary, as each person’s genome is unique and may require different levels of analysis.
The myGenome test is designed for healthy adults. For minors, we recommend the myNewborn genetic screening test, which focuses on the most common genetic conditions of childhood.
There are tests that analyze specific positions in your DNA but don't look at entire genes or the entire genome, these tests are usually cheaper and are called genotyping tests. If we were to compare them to a book, it would look something like this:
In both cases, the data is real, but the information obtained is completely different! In the first case, if we know exactly what to look for, we are likely to get interesting information, although we leave a lot of information unanalyzed, so the clinical utility is limited. It may not be visible to the naked eye in the report, but your entire genes are not analyzed in this case.
In other cases, the tests sequence the entire genome, but they do not have a team of experts in interpreting the variants, so they include in the report everything that appears in public databases without review and therefore final classification. Many of these variants have no clinical use, so the doctor cannot modify the medical treatment and causes unnecessary alarm in the healthy patient.
Longevity refers to the pursuit of maximising healthy, active years — not only extending life span but also preventing disease and maintaining quality of life.
For those interested in longevity, prevention is key: avoiding disease wherever possible, and detecting it as early as possible.
A genetic test such as myGenome reveals genetic factors that can influence health and life expectancy. This knowledge allows for:
- Development of personalised prevention strategies
- Detection of hidden hereditary disease risks
- Optimisation of lifestyle, nutrition, and medication
- Conscious planning for a long and healthy life
Genetic testing helps ensure that life is not only longer, but healthier.
myGenome is a comprehensive preventive genetic test based on whole genome sequencing, designed for healthy adults. It supports personalised health care in the following ways:
- Risk Detection: Analyses hundreds of genes linked to diseases, accurately identifying the genetic risk of inherited and multifactorial conditions (e.g. cardiovascular disease, cancer, metabolic disorders).
- Personalised Counselling: Results are interpreted by a medical genetics expert, who can advise on strategies to minimise identified risks.
- Optimised Lifestyle and Medication: Includes pharmacogenomic analysis to determine how an individual’s body processes specific medications.
- Lifelong Resource: Once performed, whole genome sequencing provides data that can be reinterpreted as scientific knowledge evolves, keeping your preventive health strategy up to date.
myGenome therefore gives everyone the opportunity to proactively take steps for their health and longevity, tailored to their own genetic characteristics.