You feel fine today. Your genome can tell you what to watch for tomorrow.
Whether you're planning for the future or want a complete picture of your genetic health — one test reads your entire genome and keeps delivering answers as science advances.
200+ clinical reports across the conditions that matter most — before symptoms appear.
Whole genome sequencing reads your complete DNA to identify inherited variants associated with disease risk, drug response, and carrier status. These are the areas where knowing early changes what you and your doctor can do.
Heart conditions that run in families.
Hypertrophic cardiomyopathy (MYBPC3, MYH7) · Long QT syndrome (KCNQ1, KCNH2) · Brugada syndrome (SCN5A) · Familial hypercholesterolemia (LDLR) · Hereditary arrhythmias
Explore conditions →Inherited variants that increase cancer risk.
BRCA1 · BRCA2 · Lynch syndrome (MLH1, MSH2, MSH6) · Li-Fraumeni syndrome (TP53) · CHEK2 · PALB2
Explore conditions →Hereditary conditions of the nervous system.
Huntington's disease (HTT) · Early-onset Alzheimer's (PSEN1, PSEN2) · Hereditary epilepsy (SCN1A) · Familial Parkinson's (LRRK2, PINK1) · Charcot-Marie-Tooth disease
Explore conditions →What you could pass on without knowing.
Cystic fibrosis (CFTR) · Spinal muscular atrophy (SMN1) · Sickle cell disease (HBB) · Tay-Sachs disease (HEXA) · Alpha/beta-thalassemia
Explore conditions →Why some medications work differently for you.
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 →Already taken a consumer DNA test like 23andMe or AncestryDNA?
An SNP array reads approximately 0.02% of your genome. Whole genome sequencing reads all of it — and your existing data can be used as a starting point.
See what it missed →"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 hereditary screening panels cover the most commonly studied genes. A Mayo Clinic study in JAMA Oncology found that standard testing guidelines missed more than half of patients with inherited mutations.
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.
The baseline you create today is the reference point every future physician works from.
One test. 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
