HEREDITARY RISK
It runs in your
family. Now you
can know if it
runs in your genes.
30X Whole Genome Sequencing. CLIA certified. Every gene in your genome analyzed for hereditary risk variants your family history suggests may be there.
CONDITION COVERAGE
If it runs in your family and has a genetic basis, WGS tests for it.
Unlike targeted panels that check a handful of genes, Whole Genome Sequencing reads your entire DNA. Every hereditary condition with a known genetic marker is covered.
20,000+ genes analyzed
Cardiac
- Brugada syndrome
- Cardiomyopathy
- Familial hypercholesterolemia
- Arrhythmias
- Long QT syndrome
Hereditary Cancer
- BRCA1 / BRCA2
- Lynch syndrome
- CHEK2 variants
- Li-Fraumeni syndrome
Neurological
- Huntington's disease
- Alzheimer's (familial)
- Epilepsy
- Ataxia
- Parkinson's disease
Connective Tissue
- Marfan syndrome
- Ehlers-Danlos syndrome
- Osteogenesis imperfecta
- Loeys-Dietz syndrome
Metabolic
- Hemochromatosis
- Wilson's disease
- Alpha-1 antitrypsin deficiency
- Familial hypercholesterolemia (1 in 250)
"They never added the numbers up until now when they saw the Dante Labs report."
Thomas, Scotland
Queen Elizabeth University Hospital Glasgow, NHS
NHS teams accept Dante data
Thomas spent years with symptoms no specialist had been able to connect. His Dante Labs Whole Genome report identified the underlying genetic cause, and his NHS clinical team used the data directly in his care pathway.
ONE TEST, ONE FAMILY
One positive finding answers the question for your whole family.
When a hereditary variant is identified in your genome, it gives every blood relative a clear, actionable reason to test for that specific variant. One genome test can change the trajectory of an entire family.
CLIA Certified
ISO 15189
NHS-Accepted
99.98% Accuracy
HOW IT WORKS
Order your kit
Delivered to your home within 48 hours. Simple saliva collection: no needles, no clinic visit.
Provide a saliva sample
Collect your sample at home and send it back in the prepaid return packaging.
ISO 15189 lab processing
Your sample is processed in our CLIA-certified, ISO 15189 accredited clinical laboratory.
200+ reports delivered
Physician-ready reports covering hereditary risk, pharmacogenomics, carrier status, and more. Updated for life.
Know what runs in your genes.
One kit, sent to your home. Your entire genome sequenced at clinical grade. 200+ physician-ready reports in 6 to 8 weeks. Updated for life as science advances.
From $449
Ships within 48 hours · Results in 6 to 8 weeks
BNPL / HSA / FSA ELIGIBLE