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.