PROACTIVE GENOMICS
Your Genome. One test. For life.
A single 30X whole genome sequence reads every base pair. 4.6 to 5M variants covering hereditary disease risk, medication response, carrier status, and more.
COMPLETE COVERAGE
What you get vs. what consumer tests read.
CONSUMER DNA TEST
~0.02%
of your genome read
~700K
positions scanned. Consumer tests use genotyping chips that read pre-selected markers. They are designed for ancestry and trait estimation, not medical decisions.
DANTE 30X WHOLE GENOME
100%
of your genome sequenced
4.6 to 5M
variants identified. Every gene, every intergenic region, every base pair. Clinical-grade sequencing at 30X depth, the standard used for diagnostic decisions.
WHAT YOUR REPORTS COVER
Hereditary disease risk
Identify inherited variants associated with cardiac, cancer, neurological, and metabolic conditions. Know your predispositions before symptoms appear.
Pharmacogenomics
132 drugs across 14 categories. Know how your body metabolizes medications before your doctor prescribes them, including 46 psychiatric medications.
Carrier status
Understand which genetic conditions you carry that could be passed to your children, even if you show no symptoms yourself.
PERMANENCE
Your test becomes more complete over time.
Your DNA does not change, but genome science is accelerating. Every month, new variant-disease associations are discovered. We validate these findings and update your reports automatically. You test once. Your genome keeps working for you.
~22%
of patients received a new clinically significant finding within 3 years
Source: HudsonAlpha CSER cohort. As science advances, previously unclassified variants are reclassified. Your genome data is automatically re-analyzed against the latest evidence.
GENOME MANAGER
More than raw data.
Your results live in Genome Manager: a secure portal where your genome becomes an active, evolving health resource.
200+ reports
Physician-ready reports organized by category: hereditary disease, pharmacogenomics, carrier status, wellness, and more.
AI interpretation
Ask questions about your results in plain language. The Genome Manager AI helps you understand what your variants mean.
Family profiles
Link family members to identify shared hereditary risks and build a multi-generational genetic picture.
Dynamic re-analysis
As new variant-disease associations are validated, your reports update automatically. No additional testing required.
DATA PROTECTION
Your genome. Your data. Your control.
Your genome is processed in our Italian laboratory under European GDPR governance, not US data frameworks. You maintain full ownership and control of your genetic information.
ISO 15189 Italian laboratory
Your sample is processed in an accredited medical laboratory in Italy, operating under the strictest European quality standards.
GDPR governed
Full European General Data Protection Regulation compliance. Your data rights are protected by the world's strongest privacy framework.
No third-party sales
Your genetic data is never sold, shared, or licensed to third parties. Not for research, not for insurance, not for any reason.
Full data control and deletion
Download, export, or permanently delete your genomic data at any time. You decide what happens to your genetic information.
The baseline you create today is the reference point every future physician works from.
One test. Your complete genome sequenced at the clinical standard used for diagnostic decisions. 200+ physician-ready reports, updated for life as science advances.
From $449
Ships within 48 hours. Results in 6 to 8 weeks.
BNPL / HSA / FSA ELIGIBLE