Complete report
A broad view of health areas, ranked follow-ups, practical next steps, and sharing notes.
Open complete sampleAn anonymised complete-report example
See a Spoke DNA Complete report before you pay.
See how Spoke turns an existing raw DNA file into clearer priorities, careful evidence context, and practical next conversations. These samples use genuine, anonymised results; explicit opt-in findings are withheld. They show the structure and depth of the service, not a promise that your report will contain the same findings.
Genuine anonymised resultsOpt-in findings withheldEvidence labels included
Built to create order, not another health to-do list.
- Prioritised
- What may matter first
- Contextual
- Evidence and limits together
- Practical
- Checks and conversations
What is inside
From signal to sensible next step.
A Spoke DNA report is designed to help you decide what deserves attention without making DNA sound more certain than it is.
- 01
A short list of what deserves attention
The plan starts with prioritised follow-ups, not a wall of genetic associations. Each item explains why it surfaced and whether it is worth acting on, discussing, or simply keeping in view.
- 02
Evidence and uncertainty in plain sight
Evidence labels, limits, and context sit beside the finding. The report separates established clinical guidance from emerging research and educational observations.
- 03
Practical next checks and conversations
You leave with sensible questions, measurements, and clinician discussion points. Your DNA is treated as one source of context, not a diagnosis or a fixed blueprint.
Priorities before detail
Know what may be worth exploring first.
Your overview brings the most useful follow-ups forward, while lower-priority and interesting findings remain available when you want the detail.
- Signals grouped into clear health areas
- Priority reflects evidence, relevance, and potential usefulness
- Important limitations stay visible beside the result
A route forward
Turn context into a better question.
Next steps are framed as options to consider: a measurement, a routine-care check, a small experiment, or a conversation with a qualified professional.
- No diagnosis from consumer raw DNA
- No deterministic claims about your future
- Clinical confirmation where a finding warrants it
Choose a sample
See the depth that matches your question.
The complete example shows the broader Complete report. The focused example shows how one area can be explored in greater depth.
Sleep, fitness & recovery
A deeper example centred on one goal, with a shorter and more targeted action plan.
Open focused sampleStart with fit, not payment
See whether your DNA file can support a useful report.
The fit check is free and private. It checks file compatibility and asks enough context to recommend the right report route before you pay.