ALREADY TESTED
You already took a DNA test. Here's what it couldn't tell you.
Upload your existing DNA data. We'll show you what it found — and the 99.98% of your genome it never read.
The Gap
Consumer tests read less than 0.02% of your genome.
23andMe
Microarray
Gene Panels
Targeted
Dante Labs
Whole Genome
Microarray chips sample a few hundred thousand fixed positions. Whole genome sequencing reads all 6.4 billion base pairs at 30x clinical-grade depth.
Blind Spots
What your test couldn't see
Consumer tests and targeted panels leave entire categories of clinically actionable variants unexamined.
Cardiac
Hypertrophic cardiomyopathy, Long QT — variants in non-coding regions
Only visible with whole genome sequencingCancer
Full BRCA1/2 coverage — not just 3 Ashkenazi variants
Only visible with whole genome sequencingNeurological
APOE4, LRRK2, hereditary neuropathies
Only visible with whole genome sequencingCarrier Status
Full carrier screening for 300+ conditions
Only visible with whole genome sequencingPharmacogenomics
132 drug–gene interactions across 14 genes, for your doctor to act on
Only visible with whole genome sequencingFree Report
See what your existing data can tell you
Upload your raw DNA file from 23andMe, AncestryDNA, MyHeritage or FamilyTreeDNA. Your report is generated in your browser session and downloads straight away — the file itself is never stored.
Your Report
Your free insight report includes
- Pharmacogenomics — the drug-gene markers your chip happened to cover
- Health-associated markers, including your APOE genotype
- Well-studied traits, from lactase persistence to caffeine metabolism
- A clear breakdown of what’s missing and why it matters
This is what <0.02% of your genome can tell you. Imagine what 100% reveals.
Dante Insight Report
Based on microarray data
Pharmacogenomics (partial)
Health-Associated Markers
Traits
What’s Missing & Why
87 additional report categories require whole genome data
Upgrade to the complete picture.
One kit, sent to your home. Your entire genome sequenced at the clinical standard used for diagnostic decisions. Physician-ready reports delivered to your Genome Manager in 6–8 weeks — permanent and updated as science advances.
Free shipping · Results in 6–8 weeks
