ALREADY TESTED
You already have DNA data
You already have DNA data. Here's what it couldn't tell you.
Standard DNA tests examine approximately 700,000 variants, which is 0.02% of your genome. Dante 30X Whole Genome Sequencing reads all 3 billion base pairs. Every gene. Every region between genes. The complete picture.
UPLOAD YOUR DATA
See what your existing data can — and cannot — tell you.
Upload your existing genetic data and we will show you exactly what your current test covers, what it misses, and what Dante Whole Genome Sequencing would add.
WHAT YOU HAVE VS. WHAT YOU COULD HAVE
Capability comparison.
CONSUMER SNP ARRAYS
~700K
variants examined
- close Pre-selected positions only
- close Misses structural variants
- close Cannot detect novel mutations
- close Not physician-grade
- close 0.02% of genome
DANTE WHOLE GENOME SEQUENCING
4.6–5M
variants identified
- check Every base pair sequenced
- check Structural variants, CNVs, indels
- check Detects novel and rare mutations
- check 200+ physician-ready reports
- check 100% of genome
THE CLEAREST EXAMPLE
BRCA: a false sense of security.
Consumer BRCA tests cover a small subset of known pathogenic variants in BRCA1 and BRCA2. A negative result on a consumer test does not rule out hereditary cancer risk. It means the specific variants they checked for were not found. The thousands of other known pathogenic variants in these genes were never examined.
Dante Whole Genome Sequencing reads the complete BRCA1 and BRCA2 genes, including intronic regions and structural variants that consumer panels cannot detect. Your results are classified using ACMG guidelines and delivered in a physician-ready hereditary cancer report.
View a sample hereditary cancer report arrow_forwardCLINICAL REPORTING
Reports your physician can act on.
200+
Clinical reports
Covering hereditary cancer, cardiac conditions, pharmacogenomics, neurological disorders, carrier status, and more. Organized by clinical category, not raw data.
Physician-ready
Outputs
Every report is structured for clinical review. ACMG-classified variants, gene-disease associations, and actionable findings presented in a format physicians recognize and trust.
~22%
New findings in 3 years
Sequence once, analyze forever. As genomic science advances, your reports update automatically. Approximately 22% of users received new clinically relevant findings within three years of their initial test.
DATA SECURITY
Your data is protected by infrastructure, not promises.
Sequencing is performed in our ISO 15189 accredited laboratory in Italy. All data processing is governed by GDPR, the strongest genetic data protection framework in the world. We do not sell your data. You can request deletion at any time.
"I was nervous about sending my DNA anywhere. Dante's GDPR protections and the fact that they process everything in Europe made it feel completely different from the US-based services. I trust them with my data."
Trustpilot Review
Verified Customer
WHAT YOU GET
Everything included.
The kit
Saliva collection kit delivered to your home. No needles, no clinic visit. Prepaid return shipping included. Results in 6 to 8 weeks.
The analysis
30X Whole Genome Sequencing. 4.6 to 5 million variants identified. Processed in our ISO 15189 accredited laboratory. 99.98% accuracy.
The platform
200+ clinical reports in your Genome Manager. Automatic re-analysis as science advances. Family management tools. Your data, accessible for life.
One test. The complete picture.
Your existing DNA data gave you a glimpse. Dante gives you the whole genome. Sequenced at clinical grade. Reported in physician-ready format. Updated for life.
From $449
Ships within 48 hours · Results in 6–8 weeks
BNPL / HSA / FSA ELIGIBLE