The complete picture of your genetic health. Clinical grade sequencing and personalized, actionable reports updated as science evolves.
Consumer DNA chips read fewer than 0.02% of them, so a discovery anywhere else never reaches their reports. We read every one, so each new finding can be checked against your whole genome.
Conditions we report on →A complete record that belongs to you, re-read every time the science moves.
Every genetic finding in 830+ reports comes with the gene it sits in, the exact base that changed, and the guideline it was classified against.
See the conditions we report on →Already TestedMost consumer DNA tests read less than 0.02% of your genome. We read all of it.See what it missed →The Most Comprehensive Genome Analysis
Proactive advice
CYP1A2 · rs762551 · C/C
Your move
Last coffee by 14:00.
Your liver clears caffeine slowly, so an afternoon cup is more likely to cost you deep sleep and push up your blood pressure.
An espresso at 15:00 is still working at midnight.
From your Nutrigenetics report
Cornelis et al., JAMA 2006HFE · p.Cys282Tyr · Homozygous
A pathogenic missense variant in HFE, on both copies of the gene. The change sits in exon 4, at the base marked on the gene below.
Explain in plain EnglishAugmented with AI
Classified against ACMG guidelines
CFTR · MONDO:0009061
Autosomal recessive
c.1521_1523del · p.Phe508del
You carry one altered copy. Recessive conditions usually only show up when both copies are affected, so this alone does not typically cause disease, but your children could inherit it.
PRS313 · z = +0.11
Higher than 54 in 100 people
30X · GRCh37
98 GB in your BAM file alone
Standard formats any genomics tool can open
BAM · FASTQ · VCF
Who We Help
Whether you are looking for answers today or protecting your health for tomorrow, a complete read of your entire genome is the only place to start.
Proactive Health
Whole genome sequencing gives you the complete genetic picture now — so you and your doctor can decide before anything becomes urgent.
Learn moreHereditary Risk
Your genome contains inherited variants associated with cardiac, cancer and neurological conditions. We read all of them — with the clinical depth to give the result meaning.
Learn moreUnexplained Symptoms
Standard diagnostic tests check for a pre-selected set of answers. We sequence your full DNA — including the parts no test was designed to check.
Learn moreTreatment Not Working
Your genes determine which treatments are most likely to work — and which are not. We give your doctor the evidence to inform your plan.
Learn more
The Kit
A single sample, collected at home. Your whole genome is sequenced at 30X in accredited laboratories and held as a permanent record — every new report the science produces is read from it, without a second test.
From $449
Order your kitHSA/FSA eligible
Accredited laboratories · Reports updated as the science advances · Your data is always yours
Consumer genotyping chips read under 0.02% of your genome. We sequence all of it at 30X depth in accredited laboratories, which is what makes a variant a finding a clinician can act on.
30X
Coverage gold standard
5M
Variants identified per test
830+
Clinical grade reports
99.98%
Sequencing accuracy
Accredited by & published in
Hereditary screening
Hereditary conditions travel down families. Whether you're planning a family or already have one, reading your whole genome shows what could be passed on, so the next generation starts with answers rather than surprises.
In Their Words
A family history of cancer. A diagnosis no one could explain. A family on the way. Hear why they chose to read their whole genome, not a sample of it.
Every Year
Your DNA does not change, but what science knows about it does. As each new finding is published, we check it against the sequence you already gave us and turn it into new insight in your reports — no new sample, no second test.
The Process
Free delivery worldwide.
Simple finger-prick blood spot collection at home. Takes 5 minutes. Everything you need is in the kit.
Pre-paid return label included. Drop it in any post box.
Reports delivered to your Genome Manager in 6–8 weeks. Review every finding and share directly with your physician.
Optional add-on
Not part of the genome test. A separate membership that sends a blood spot card twice a year, showing what is changing at the cellular level — which your genome never does.
Cellular Monitoring →
“They never added the numbers up until now, when they saw the Dante Labs report.”
Whole Genome Sequencing
From $449
Whole genome at 30X, sequenced once and yours for life
90+ condition and wellness reports and 30+ polygenic risk scores included. 760+ condition and wellness reports and 60+ polygenic risk scores with Premium: $99 for the first year, then $99 a year.
HSA/FSA eligible
→
As seen in & research partnerships
Premium access with 800+ actionable, physician-ready reports, on hereditary risk, drug response and carrier status — and every new report the science produces, for as long as you hold the data.
