Private Genome Action Plan
Your raw DNA, distilled into clear priorities, practical next steps, and what is safe to ignore for now.
Spoke DNA turns your existing 23andMe, AncestryDNA, MyHeritage, Living DNA, or other supported raw DNA file into a private Genome Action Plan: what looks worth checking, what can wait, and what is only background. Evidence-weighted, clinician-grounded, and built for decisions you can take at home, track over time, or discuss when it matters.
Educational, evidence-reviewed reports. Not diagnosis, treatment advice, or a replacement for clinical testing.
“For the first time, my DNA results felt useful instead of overwhelming. I knew what to do next, and what not to worry about.”
Pricing · One-time fee, no subscription
Genome-informed. Context-led. Action-focused.
Single health area
Best for one specific concern.
Full Genome Action Plan
Best balance of depth and price.
Cancel any time before processing for a full refund. Reports are educational — not a diagnosis, not treatment advice. Read our guardrails →
Inside a Spoke report
Open a full sample report to see how Spoke turns raw DNA into clear priorities, practical next steps, clinician-friendly context, and findings you can safely leave in the background.
See what gets checked, tracked, discussed, and ignored for now.
Genome Action Plan
Evidence & safety framework
A Spoke report shows why a finding appears, how strong the evidence is, what kind of claim it is, and what it should not be used for. Built around four hard rules.
Founder-led interpretation, evidence labels, and clear safety lines — visible enough to trust, quiet enough to keep the page moving.
Source, format, genome build, coverage — checked before any signal is reportable.
Clinical guidelines and drug-gene resources outrank isolated SNP-trait claims.
Stronger, moderate, emerging, educational — every finding carries its label.
What it may mean, what it does not prove, what must be discussed with a clinician.
FAQ
Plain answers to the questions we get most often.
No. Spoke does not predict whether you will get cancer, Alzheimer's, or any other condition. Sensitive areas such as cancer context, Alzheimer's, Parkinson's, and psychiatric traits are opt-in only. If you choose to include them, they are handled as limited, non-diagnostic context: clearly labelled, separated from everyday actions, and never framed as a standalone fear-led module.
23andMe, AncestryDNA, MyHeritage, Living DNA, and other raw DNA files we can validate during the fit check. We're adding Nebula and Dante Whole-Genome support in Q3 2026. If you've lost your file, we'll walk you through re-downloading it from your provider.
Focus reports return in 3–4 business days. Complete reports return in 5–7 business days after intake and file checks are complete.
Yes, if that is useful for you. The main report is written for you first: clear priorities, evidence labels, and practical next steps you can act on or track. When a finding is worth discussing, we include a concise clinical summary you can print, save, or attach to your patient portal.
Stored encrypted, used only to generate your report and any updates you request, never sold, never shared with insurers. One click in the portal deletes everything — file, derived data, and report. Receipts of deletion are emailed to you.
No. Spoke reports are educational, designed to inform clinician discussion. Any clinical decision — medication, screening, surgery — requires confirmation through measured tests and a qualified healthcare professional. We say so on every page.
Coming soon
We are opening the first report cohort carefully. Leave your name and email and we will follow up when the next places are ready.
Start when you're ready
Cancel before processing for a full refund. Reports are educational, not a diagnosis.
