Upgrade your health.
For the rest of your life.
A Discover which diseases you may be at risk for in the future.
B Learn which medications may be less effective for you and require dosage adjustments.
C Give your doctor the ability to personalize your treatment based on your DNA.
1 Order a collection kit on our website or pick one up at a collection point. Collect a saliva sample or a drop of blood from your finger.
2 Submit your sample at a collection point or send it to us by courier (coming soon).
3 Within about six weeks, you'll receive a detailed medical report and recommendations.
4 Every year, you'll get an updated report based on the latest scientific knowledge.
1 Risk assessment for more than 150 genetic diseases.
2 Information about your ancestry, including Y and mtDNA haplogroup analysis.
As a certified medical facility, we maintain strict medical confidentiality and comply fully with GDPR regulations.
Our collection kits are registered with SÚKL, and results are evaluated by qualified geneticists.
Your health data is stored anonymously in encrypted, offline form—and it remains your property.
One DNA analysis with a one-year membership.
Plan includes:
Three-year membership with advanced features.
Plan includes:
Five-year membership with all premium features.
Plan includes:
Some competitors claim to give health advice even though their tests lack clinical validity or accuracy.
They often operate illegally and perform tests incorrectly. Check if they are a healthcare facility and if their kits are IVD certified — they usually are not.
Our facility is fully certified, and our kits are authorized.
Our results are accepted by doctors and other healthcare professionals.
Investigate the competition to determine if they are a valid clinic and their collection kits registered.
Competitors often sequence only 1% of your DNA (e.g., exomes) and may outsource processing abroad without proper analysis.
They may not know which devices performed sequencing or how results were evaluated, as they outsource samples abroad and pass on results without full analysis.
We sequence your entire genome, without PCR, at 30x coverage. We process sequences ourselves, and our doctors perform the evaluation.
Sequencing the entire genome is essential for detecting diseases caused by mutations outside genes.
Avoiding PCR is important for detecting rare conditions, where PCR can introduce errors.
30x coverage means each base of your genome is read 30 times.
Ask competitors how much of the genome they sequence and at what coverage.
Competitors often deliver reports without clear conclusions.
They may state that a mutation exists on a certain gene but omit its position or the number of reads confirming it, making it impossible to rule out sequencing errors.
These reports are more like genetic horoscopes.
We deliver a comprehensive medical report with all the details needed by you and your healthcare providers.
Ask competitors whether their reports include coverage information for each mutation.
Competitors often give a one-time report and basic lifestyle tips, and that's it.
We securely archive an electronic copy of your genome so you can receive updated reports without repeat sampling.
Your DNA doesn't change, but science does — allowing us to continually provide new insights.
You will receive an evaluation of your risk for over 150 genetic diseases, plus information about your ancestry through Y and mtDNA haplogroup analysis. Additional insights about your DNA are added continuously during your membership, and at least once a year you will receive an updated medical report.
Yes. During registration, you will complete an ethical questionnaire where you can choose whether or not to learn about predispositions to currently incurable diseases. You can also choose not to learn whether you carry a genetic risk that could be passed to the next generation. You can read more in our Ethics Board section, in our code of ethics, and in the ethical questionnaire.
Read the report carefully, then follow the recommendations provided. Prevention, overall health management, and lifestyle are key. If you want more information, you can contact our doctor for additional details and recommendations.
Stay calm. If there is an increased risk of a particular disease, our geneticist will recommend the next steps and guide you through the process.
Our DNA test uses whole genome sequencing (WGS). This advanced technology analyzes your entire DNA sequence (100%) with high accuracy. Unlike most competitors who test only certain genes or exome regions (about 0.1%), WGS reads your complete genetic code — over 3 billion DNA bases. The biggest advantage of WGS is that, as genetic research advances, your complete genome can be re-analyzed without collecting new samples. We can provide you with new insights regularly, based on scientific progress, without the need for another collection.
Collection is done only once. Depending on your chosen membership, you will receive an updated medical report every year, with new scientific findings and recommendations.
We use PCR-free library sequencing on the NovaSeq X Plus platform with 30x coverage.
This is one of the most accurate sequencing methods available. Each part of your genome is sequenced multiple times to minimize errors and increase accuracy. Our standard is to achieve an average coverage of 30 reads per base.
There are no biological age restrictions, but for ethical reasons we currently test only individuals aged 18 or older.
Your biological sample is destroyed once the analysis is complete. If your membership includes archiving, the digital DNA data is stored securely. Archived DNA is deleted automatically at the end of your membership. You can also request deletion at any time. All DNA is stored anonymously in encrypted, offline form, and remains your property.
Yes. Purchase a collection kit and inform the recipient to register their sample on our portal.
Submit the sample at a collection point or hand it to the courier within 48 hours of collection.
While sample collection takes only a moment, analysis takes time. The delivery timeline depends on:
We use the highest security standards to prevent failures at the system, employee, or company level. After archiving, your DNA and results exist only in two places — in our DNA bank and on your DNA carrier — both encrypted and stored in geographically separate locations to ensure recovery in case of disaster.
Log into the portal and visit the Results section.
Yes, you can buy tests for multiple family members. However, we do not recommend testing individuals under 18 years of age. Each family member must register their own kit. Label each kit with the family member's name to avoid mixing samples.
Instructions are included in the kit box, printed in the paper manual, and available as a video tutorial on our customer portal.
You may submit the sample at a collection point without prior registration. However, without proper registration, you will not receive your analysis or report. If you submit an unregistered sample, we will request your email address and send you instructions to complete registration. If sending by courier, the kit must be registered before shipment.
The DNAmeter collection point is an automated station where you can pick up a DNA collection kit and submit your sample if you prefer not to use our courier service. It keeps samples stored safely under proper conditions before analysis. You can find a list of our collection points here.
You can find our collection points here.
It is rare, but if it happens: we will contact you, send a new collection kit free of charge, and request a new sample.
Yes. The results are your property and can be shared with your family or doctor. You can share them online via our portal or download them as a file. The results and recommendations we provide are for informational and educational purposes only. For diagnostic purposes, always consult your doctor!
