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If you suffer from clinical symptoms of unknown reason or have a positive family history of any suspected hereditary disease, genomic testing can provide answers and make a precise diagnosis, in order to find certainty and start timely treatment.

With myLifeDNA™, we sequence your entire genomic DNA and interpret selected genes based on your clinical symptoms as well as personal and family medical history. After every analysis, you will receive a detailed report with further information and action points. myLifeDNA™ also includes a subscription to bi-annual updates of your results based on most recent scientific knowledge.

Highest-quality interpretation of your genomic data

Analysis of genes based on specific symptoms and positive family history

Includes a pool of more than 20,000 genes

Bi-annual updated results based on scientific knowledge

Access to professional genomic counseling

Sampling-Kit and global free shipping included

Regular updates

Bi-annual updates of your genomic results based on the most recent scientific knowledge.

Incidental findings

With your consent we report previously unknown genomic results in specific genes that have a treatment consequence but are not related to your potential clinical symptoms.

Easy to understand

Results and recommendations are presented in a suitable way for non-medical people and more in-depth for genomic experts.

More than 500 million people globally are suffering from a genomic disorder. An early diagnosis is critical to bring the most benefit to the quality of life and the overall prognosis of these patients.