It runs in your family. Now you can know if it runs in your genes.
Whether a recent diagnosis brought you here or a question you've carried for years — knowing which variants you carry gives you and your doctor the chance to screen earlier and plan ahead.
If it runs in your family and has a genetic basis, Genome Test helps you discover it.
Early discovery means earlier screening, targeted monitoring, and informed decisions for you and your family. These are the condition categories most commonly carried across generations.
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 →Conditions that standard testing misses.
Marfan syndrome (FBN1) · Ehlers-Danlos syndromes (COL5A1, COL5A2) · Osteogenesis imperfecta · Loeys-Dietz syndrome · Noonan syndrome (PTPN11)
Explore conditions →Inherited disorders affecting organ function.
Hereditary hemochromatosis (HFE) · Wilson's disease (ATP7B) · Alpha-1 antitrypsin deficiency (SERPINA1) · Familial hypercholesterolemia (1 in 250 are carriers)
Explore conditions →"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.
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. Her doctor selected an alternative — and she started effective treatment from day one.
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
One positive finding answers the question for your whole family.
If this test identifies a variant associated with a heritable condition, every blood relative has new information. That is not just one test for you alone — it is one test for your family.
A single whole genome sequencing result can inform the health decisions of parents, siblings, and children — giving each of them clarity that would otherwise require separate testing.
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.
Know what runs in your genes.
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
