Discover Your Genome
The answer was always in your DNA.
Until now, the most important information about your health has been sitting in your DNA — unread. Dante Labs sequences your entire genome and turns what it finds into answers you can act on.
As seen in & research partnerships
Who We Help
Every genetic question deserves a complete answer.
Whether you are investigating a hereditary condition, searching for an explanation your doctors haven’t found, or simply want the most complete view of your health — whole genome sequencing is the starting point.
HEREDITARY RISK
A family history you want to understand.
Cancer, cardiac conditions, neurological disorders — if it runs in your family, your genome holds the map.
Learn more →
UNEXPLAINED SYMPTOMS
When nobody can tell you what's wrong.
Years of tests with no answers. Whole genome sequencing finds what targeted panels miss.
Learn more →
TREATMENT NOT WORKING
Your medication should work — but it doesn't.
Pharmacogenomic analysis reveals how your DNA affects drug metabolism, efficacy, and adverse reactions.
Learn more →
PROACTIVE HEALTH
You're healthy. You want to stay that way.
Identify risks before symptoms appear. Actionable insights for nutrition, fitness, and preventive care.
Learn more →Already Tested
You already took a DNA test. Here’s what it couldn’t tell you.
Clinical-grade results. Chosen by individuals, trusted by doctors for their most complex cases.
30X
Whole genome coverage
5M
Variants identified per test
200+
Customized clinical reports
99.98%
Sequencing accuracy
“They never added the numbers up until now when they saw the Dante Labs report. That one test changed everything for Thomas and his care team at NHS.”
One Test
What sequencing your entire genome actually means.
Your full DNA (not just a part of it)
Consumer tests read ~0.02% of your genome. We sequence all 6.4 billion base pairs at 30x clinical depth — exons, introns, regulatory regions, everything.
Comprehensive insights and specialized reports
Over 200 reports covering hereditary cancer risk, cardiac conditions, pharmacogenomics, carrier status, rare disease markers, and more — reviewed against clinical databases.
Your test becomes more valuable every year
Your genome data is yours forever. As science advances and new variants are classified, your reports update automatically — no retest needed.
The Process
Four steps to get started. No clinic visit required.
Step 01
Order your kit
Choose your test and complete checkout. Your collection kit ships within 48 hours.
Step 02
Collect your sample
Follow the simple instructions to provide a saliva sample at home. Takes under 5 minutes.
Step 03
Ship it back
Use the prepaid return label. Your sample goes directly to our CLIA-certified lab.
Step 04
Get your results
Receive 200+ physician-ready reports in your secure portal within 6–8 weeks.
Patient Outcome
‘They never added the numbers up until now when they saw the Dante Labs report.’
Thomas, Scotland
Queen Elizabeth University Hospital Glasgow, NHS
After years of unexplained symptoms and inconclusive targeted tests, Thomas’s clinicians ordered whole genome sequencing through Dante Labs. The report identified a combination of variants across multiple genes that, together, explained his condition — something no single-gene panel had ever surfaced. His care team at Queen Elizabeth University Hospital Glasgow used the findings to adjust his treatment plan within weeks.
Read more clinical outcomes →One test. A lifetime of answers.
Your genome never changes, but science does. Order once and receive updated reports as new discoveries are made — at no additional cost.
From
$449
Ships within 48 hours · Results in 6–8 weeks
