Genetic testing
Our testing is aimed at identifying pathologically significant regions and important genetic risks that are not covered by other similar consumer tests.
The testing includes markers for in-depth health analysis and rare genetic features.
The results will help you better understand your genetic features and risks. This creates a foundation for personalized diagnostics, prevention, and correction, and helps you manage your health more consciously.
The research method is SNP genotyping on a modern chip platform. Analysis and presentation of results are performed using the 2026 version of the human reference genome.
Access to raw data is included in the testing cost.
RAW data is available in your personal account and is provided in GRCh38 (hg38) coordinates compatible with modern databases and interpretation tools.
You can download it and use it for further analysis.
You will be able to explore the data on your own or share it with doctors and relevant specialists for deeper analysis.
Please note: the testing price already includes access to all books and 7+ reports available on the site. Details here.
Materials will be available in your personal account immediately after payment.
- Sending the kit: after payment confirmation, we send you the test kit.
- Collecting and sending the sample: take a sample (a cheek swab from the inside of your mouth) and send it according to the instructions
- Analysis: the average duration of the analysis is 4–8 weeks from the moment the sample is received in the laboratory.
- Receiving results: results will be available in your personal account together with all additional materials and reports. You will also be able to download the results (RAW data) in your personal account.
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