Your results came back normal. The answer may be in your DNA.
Whether your tests keep coming back normal or you're just beginning to wonder — your question deserves a more complete answer. Whole genome sequencing reads your entire DNA, giving you and your doctor a clearer, more complete picture to work from.
When your question has a genetic basis, Genome Test can help you find the answer.
A clearer picture means better conversations with your doctor — and a path toward answers that standard evaluations alone may not provide. These are the areas where genomic insight matters most.
When no test has found an answer.
Unexplained connective tissue symptoms, hypermobility, vascular fragility, skeletal differences, or recurring features across multiple body systems that don't fit a single clinical diagnosis.
Explore conditions →Symptoms without a clear diagnosis.
Unexplained seizures, neuropathy, cognitive changes, movement disorders, or progressive neurological decline with no identified cause — investigated across all known neurological-associated genes.
Explore conditions →Disorders affecting organ function.
Unexplained iron overload, liver dysfunction, persistently elevated cholesterol, or metabolic symptoms that don't respond to standard management — traced to their genetic origin.
Explore conditions →Inflammation with a genetic origin.
Recurring fevers, unexplained swelling, chronic inflammation, or autoimmune-like patterns that don't respond to standard treatment — investigated for monogenic inflammatory causes.
Explore conditions →Why your medication may not work.
Your DNA affects how you respond to 132+ drugs — including antidepressants, pain medications, blood thinners, and chemotherapy agents. Pharmacogenomic variants explain why standard doses fail.
Explore conditions →You have a diagnosis, but your treatment isn't improving things.
That's a different question — and a different answer. Your genetic subtype may determine which treatment works best.
See how whole genome sequencing informs treatment →"They never added the numbers up until now when they saw the Dante Labs report." — Thomas, Dante Labs patient
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.
Twenty years old. Years of conflicting opinions. One answer.
Angela had spent years navigating conflicting medical opinions with no clear diagnosis. Standard tests had not identified a cause. Dante Genome Test identified a rare genetic variant that explained her symptoms — giving her and her medical team the clarity to move forward with an informed care plan.
What sequencing your entire genome actually means.
Standard diagnostic tests check for a pre-selected set of answers. When they come back negative, the investigation often stops — not because the answer doesn't exist, but because the test wasn't designed to find it.
Your full DNA (not just a part of it)
Traditional genetic testing looks at narrow sets of genes, missing most parts of your genome. We sequence your full genome — every gene and every region between genes.
Comprehensive insights and specialized reports
Easy to read and with answers you and your doctor can act on. Not a file to interpret – 200+ clinical reports, organized by category.
Your test becomes more valuable every year
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. Your test becomes more valuable every year.
Clinical-grade results. Chosen by individuals, trusted by doctors for their most complex cases.
Accredited by & published in
Four steps to get started.
No clinic visit required.
Order your kit
Ships within 2 business days. Free delivery worldwide.
Collect your sample
Simple saliva collection at home. Takes 5 minutes. Everything you need is in the kit.
Send it back
Pre-paid return label included. Drop it in any post box.
Access your results
Reports delivered to your Genome Manager in 6–8 weeks. Review every finding, ask questions, and share directly with your physician. Your data is stored permanently.
Your symptoms are real. The answer may be in your genome.
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
