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Genetics
Report
Complete genome sequencing that reveals inherited susceptibilities and genetic risks. It aids in targeted prevention and conscious health preservation.
Price:
1,450,000 HUF
Overview
Get to know how your body works
The Genetics Report provides a comprehensive overview of your genetic makeup through whole genome sequencing. We reveal your inherited traits, disease predispositions, and genetic risks. We provide detailed analysis of clinically relevant genes, polygenic risks, genetic diseases, and carrier status. We show how your body responds to certain medications (pharmacogenomics), helping you choose optimal pharmacological treatment. You will receive the results in the form of personalized health and lifestyle recommendations, allowing you to make informed decisions about prevention and treatments.
Include
What does our service include?
Clinically relevant gene panel
We identify genes associated with diseases and treatments, thereby supporting their prevention.
Carrier status analysis
We will reveal any potentially heritable genetic diseases, hereditary variations, thus supporting lifestyle and family planning.
Complete genome sequencing
About 99% of the tested DNS can be analyzed in this way, which is considered the most modern procedure in genetics.
Polligénes risk assessment
Let's analyze the risk of diseases caused by multiple genes, such as heart diseases and certain types of cancer.
Personal consultation
We provide personalized recommendations for lifestyle, diet, and prevention based on genetic results.
Pharmacogenomics
Based on your genetic characteristics, we will examine how different medications and preparations affect your body, and we will make recommendations for their use according to active ingredients.
Recommendation
Who do we recommend the Genetics Report for?
We recommend this to anyone who wants to explore their inherited tendencies and risks. If you are curious about which diseases you might be genetically predisposed to, or if you want a personalized prevention strategy, this test is essential. It is especially useful before starting a family or if hereditary diseases have already occurred in your family.
Process
This is how we help you step by step on your health journey
Our processes are personalized. Instead of thinking in templates, we truly pay attention to you, we only examine what is necessary and guide you along the path to your health.
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Data collection
We will discuss with you and analyze the most important medical history data to understand your health condition.
Expert consultations
To create your personal database, we collect information about you during consultations to ensure the most accurate outcome.
Sampling
We will carry out the necessary sampling, laboratories, and tests so that your data is available for the next steps.
Data analysis
After the arrival of the data, each professional team analyzes and connects the information according to their chosen field and then collectively.
Report handover
We will present your report to you in a calm environment, clearly, and in detail.
