The complete picture of your health.
Get a full genetic understanding of your health. Guide your prevention with precision. Finally address symptoms other tests couldn't explain. We sequence your entire genome — not the 0.02% most DNA tests examine.
A lifetime of clinical insights from a single test.
Get actionable genetic reports. User friendly portal organized by clinical area. 30X Genome Test. Full data ownership and privacy protection.
200+ Physician-Ready Reports
Comprehensive reporting across cardiology, oncology, rare disease, neurological conditions, and pharmacogenomics — designed to share directly with your specialist, and continually updated for life as science advances.
Secure Genome Manager
A HIPAA and GDPR-compliant portal with lifelong access to your complete clinical insights, new report releases as science advances, and specialist referral guidance.
30X Clinical Sequencing
Your entire genome sequenced at 30X coverage — the standard required for clinical-grade diagnosis. Every one of your 6.4 billion letters, read.
Full Data Ownership & Privacy
Unrestricted access to your BAM, VCF, and FASTQ files. Your genetic data belongs to you — export it to any independent specialist, at any time, forever.
Dante's secure data architecture was built across multiple, independent GDPR and HIPAA-compliant data protection layers. Your data is never shared with insurers, pharmaceutical companies, or research programs without your explicit consent. You can request deletion at any time.
Full data and privacy policy →Standard genetic tests miss 99.98% of your DNA. Dante reads all of it — so nothing clinically relevant goes unseen.
Every genetic question deserves a complete answer.
Whether you are searching for answers today or protecting your health for tomorrow, a complete read of your entire genome is the only place to start.
It runs in your family. Now you can know if it runs in your genes.
Your genome contains inherited variants associated with medical conditions like cardiac, cancer, and neurological. We read all of them — with the clinical depth to give the result meaning.
Learn more →When traditional lab tests say you're fine. And you know you're not.
Standard diagnostic tests check for a pre-selected set of answers. We sequence your full DNA — including parts that no test was designed to check. If the answer is in your genome, we will help you find it.
Learn more →Your diagnosis may be right. Your treatment plan may be incomplete.
Your genes determine which treatments are most likely to work — and which are not. We give your doctor the tools and insights to inform your treatment plan.
Learn more →You want to know before something forces the question.
Some people don't wait for a diagnosis or a family history to act. Whole genome sequencing gives you the complete genetic picture now — so you and your doctor can make informed decisions before anything becomes urgent.
Learn more →You already took a DNA test. Here's what it couldn't tell you.
Most consumer DNA tests read less than 0.1% of your genome. We read all of it.
Learn more →The conditions your genome reveals — from cardiac, to rare disease, to cancer risks.
Most tests only check where they’re told to look. We sequence your entire genome — which means we find what no targeted test was built to detect, across every category of genetic risk.
Heritable heart conditions
Inherited cardiomyopathies, arrhythmias, and familial hypercholesterolaemia — where early genetic identification changes outcomes for entire families.
Explore conditions →Hereditary cancer risk
BRCA1/2, tumor suppressor genes, and thousands of cancer-risk markers — well beyond what standard panels test for.
Explore conditions →Brain and nervous system risk
APOE4 and Alzheimer's risk, LRRK2 and hereditary Parkinson's, ALS — identified before symptoms force the question.
Explore conditions →Answers for diagnostic odysseys
Unexplained developmental delays and thousands of rare metabolic disorders — conditions where targeted tests return no answer.
Explore conditions →Drug response from 132 medications
How your genes affect your response to antidepressants, statins, and more. Precision prescribing instead of trial-and-error.
Explore conditions →When every test comes back normal
Your genome may contain the answer that no targeted test was designed to find.
Explore conditions →The results doctors bring to their hardest cases.
"You save lives." — Dante Labs customer
Forty years of uncertainty. One test.
A patient had spent decades in the UK healthcare system without a diagnosis. Dante data, accepted by NHS clinical teams at Queen Elizabeth University Hospital Glasgow, identified Noonan Syndrome and a RUNX1 leukemia-associated variant that had gone undetected. After 40 years, they finally had an answer.
A complete read delivers a complete picture.
A patient came to Dante to investigate periodic paralysis. Reading the complete genome identified a concurrent hereditary cardiac finding — Brugada syndrome — that their doctor confirmed with an ECG. The result also explained a family member's unresolved cardiac history. One test. Every answer in it.
Sequenced in 2019. The data worked in 2021.
Jennifer sequenced her genome with Dante two years before her breast cancer diagnosis. When treatment began, Dante's pharmacogenomics data showed her prescribed chemotherapy would cause serious adverse effects based on her genetic profile. Her doctor selected an alternative — and she started effective treatment from day one.
Accredited by & published in
One test.
A lifetime of answers.
One kit, sent to your home. Your entire genome sequenced at the clinical standard used for diagnostic decisions. 200+ physician-ready reports delivered to your Genome Manager in 6–8 weeks — permanent and updated as science advances.
Ships within 48 hours · Results in 6–8 weeks
