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 \u2014 and what 99.9% of your genome it never read.

Upload your dataOrder full genome test →
CLIA CertifiedCAP AccreditedISO 15189 Medical LabACMG ClassifiedHIPAA & GDPR100,000+ Genomes Sequenced

The Gap

Consumer tests read less than 0.1% of your 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 sequencing

Cancer

Full BRCA1/2 coverage — not just 3 Ashkenazi variants

Only visible with whole genome sequencing

Neurological

APOE4, LRRK2, hereditary neuropathies

Only visible with whole genome sequencing

Carrier Status

Full carrier screening for 300+ conditions

Only visible with whole genome sequencing

Pharmacogenomics

132 drug-gene interactions your doctor can act on

Only visible with whole genome sequencing

Free Report

See what your existing data can tell you

Upload your raw DNA file from 23andMe, AncestryDNA, or any microarray provider. We'll generate a free insight report and email it to you.

Drop your DNA file here or click to browse

.txt or .csv from 23andMe, AncestryDNA, MyHeritage

Your data is encrypted and never shared. We use it only to generate your report.

Your Report

Your free insight report includes

  • Ancestry composition from your existing data
  • Carrier status for variants detectable by microarray
  • Limited pharmacogenomics (the handful your chip tested)
  • A clear breakdown of what’s missing and why it matters

This is what <0.1% of your genome can tell you. Imagine what 100% reveals.

Dante Insight Report

Based on microarray data

Ancestry Composition

Carrier Status (limited)

Pharmacogenomics (partial)

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. 200+ physician-ready reports delivered to your Genome Manager in 6–8 weeks — permanent and updated as science advances.

From $449

Ships within 48 hours · Results in 6–8 weeks

Order your Genome Test