Comprehensive genetic analyses identify possible hereditary predispositions for a set of most common diseases. Based on the results, the level of risk for cardiovascular, cancer, metabolic, autoimmune and other diseases can be determined and appropriate preventive measures can be set in consultation with a doctor.
Predictive genetics aims to detect gene variants associated with the risk of a specific disease before it first manifests, allowing a comprehensive view of the area and effective targeting of prevention. Predictive genetics is the ideal tool to optimize your health and lifestyle.
If there are certain diseases in your family, genetic analysis can help you discover their cause and set up appropriate preventive measures. If you are suffering from an unspecified health problem, the results of the genetic analysis may recommend appropriate treatment. If you want to make the most of your health, predictive genetics will give you a head start and keep you healthy into old age.
GenScan® analysis is a modern and accessible tool for personalized prevention. It can uncover health risks hidden in your DNA, allowing you to take necessary preventive measures and avoid the development of diseases, or start appropriate treatment before the disease fully manifests. With GenScan®, you can gain an advantage in caring for your health, improve your quality of life, and maintain your health into old age.
The result will be delivered within 6 months.
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GenScan® INDIVIDUAL analysis is a modern and affordable tool for personalized prevention. It brings the unique opportunity to choose only the areas that interest you the most. Focus your prevention and health care in the right direction.
The result will be delivered within 6 months.
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The BRCA1,2,Screen® genetic analysis examines the 34 most common mutations in the BRCA1 and BRCA2 genes which cause breast and ovarian cancer in women and increase the risk of prostate cancer in men. These genes are inherited independently of gender, so prevention is absolutely key across the population. This test is recommended for basic prevention, it is not a substitute for a complete BRCA1,2 gene test.
You will receive the result within 15 working days.
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The PharmaGen® test detects variants in genes that affect the metabolism of commonly used drugs, particularly in the fields of psychiatry, neurology and internal medicine. Our genetic predisposition influences the rate of drug breakdown, its concentration in the blood, the effectiveness of treatment and the risk of side effects. Simply put, genetic analysis can help you find out what medication is right for you and at what dose, and which drugs to avoid, which can significantly speed up the appropriate treatment and increase its effectiveness.
You will receive the result within 10 working days.
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The TromboGen® genetic analysis can detect innate predispositions to increased blood clotting and allows you to take the necessary preventive measures in time. Thrombosis is a blood clot that can cause serious health complications, in extreme cases even death. It is caused by slowed blood flow and/or altered blood composition due to the joint effects of external risk factors and hereditary predispositions.
You will receive the result within 10 working days.
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The TromboGen Gravidity® genetic analysis can detect risk predispositions for increased blood clotting, which can significantly contribute to reducing the risk of thrombosis and related pregnancy complications. Pregnant women are at risk of developing thrombosis, or a blood clot, much more than other women. This is due to the physiological changes that occur during pregnancy and possible hereditary dispositions.
You will receive the result within 10 working days.
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The CardioGen® test can detect the risk of cardiovascular disease before the first clinical symptoms appear. Cardiovascular disease, or heart and blood vessel disease, is one of the so-called genetically determined diseases of affluence, the likelihood of which increases with age. Therefore, prevention plays a crucial role here.
You will receive the result within 10 working days.
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Periodontitis is an inflammatory disease of the supporting structure for the teeth called the periodontium. The cause is a combination of the presence of certain strains of bacteria in dental plaque and the immunological or genetic predisposition of the patient. The bacterial and genetic examination DentalScan® detects both of the above-mentioned risk factors for periodontitis, which can significantly contribute to early diagnosis, the selection of optimal treatment or the adoption of appropriate preventive measures.
You will receive the result within 15 working days.
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The gut microbiome influences virtually the entire body, from nutrient digestion and energy absorption to immune system activity, liver function and risk of various diseases, and even the psyche. By genetically analysing a small stool sample in the laboratory, the types and amounts of bacteria that live in your colon can be determined. Together with an analysis of dietary habits, it is then possible to deduce what substances in the intestines are produced by the activity of the bacteria and how this affects the body. In addition, if we know what these bacteria need to multiply or what is not good for them, we can adjust the amount of bacteria in our gut through our diet. In this way, we can influence their impact on our body - and on our physical and mental health.
You will receive the result in 4-6 weeks.
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More info9 900 Kč
An examination of your gut microbiome will show you whether your gut bacteria are in balance and working with your body to maintain a good immune system. A biochemical blood test will reveal whether you are already developing certain risk factors and whether you are lacking any essential nutrients.
The examination includes an assessment of your eating habits and a consultation with a specialist who will make precise recommendations to ensure that the prevention is effective.
The most comprehensive genetic analysis that analyses approximately 4,500 genes that are associated with various inherited diseases and birth defects. It helps diagnose the cause of rare inherited diseases. Based on the results, a prognosis can be determined, a prevention or treatment strategy can be developed and the risk of recurrence of the same disease for blood relatives can be assessed.
You will receive the result within 6 months.
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More info82 000 Kč