Every Geneprint programme translates genomic, clinical and blood-based biology into one clear, physician-reviewed set of deliverables — each with an explanation and a next step.
A visual summary of the cancer types relevant to you and your current risk category for each.
Pathogenic and likely pathogenic variants, explained in plain language, with their clinical implications.
Which tests, from what age, and how often — based on your own profile, not a generic checklist.
The specific, realistic actions most likely to reduce your risk, in priority order.
Every significant finding is mapped to one clear next step.
A single, physician-reviewed report bringing every finding together.
Ongoing, secure access to your results, actions and history.
Ask plain-language questions about your own report, any time.
A full year of portal access, reminders and updates — not a one-time download.
Updated history and AI reinterpretation, with a new blood draw where recommended.
Pathogenic or likely pathogenic variants are reported together with the related hereditary cancer syndrome, associated cancer risks, any confirmation requirements, and a recommended specialist referral where relevant. We also note potential implications for biological relatives and whether targeted family testing should be considered.
Variants of uncertain significance are never used to recommend major preventive procedures, or to classify someone as having a hereditary cancer syndrome.
The cancer types assessed for your profile, your current risk category for each, the principal drivers behind that estimate, the recommended level of attention, and the screening actions it connects to.
Which tests are recommended, when to begin, how often to repeat them, and whether you are due, on schedule or overdue. Geneprint follows applicable national and hospital guidance — established screening remains central, and your programme personalises it rather than inventing new tests.
Screening is never recommended simply because a test exists: screening itself can cause harm through false positives and overdiagnosis, so enhanced screening or specialist management is suggested only where it is warranted.
A ranked, specific and clinically realistic list linked to your own profile — not generic wellness advice. Depending on your findings, this may include smoking cessation, alcohol reduction, weight management, physical activity, metabolic health, UV protection, HPV vaccination, hepatitis-related prevention, exposure reduction, or hormonal and chronic-condition management.
A summary of your metabolic health, inflammatory context, and relevant protein and metabolite patterns, together with any areas requiring clinical attention. This forms a baseline for comparison at your next annual reassessment.
Always framed as biological context, never as an independent cancer diagnosis.
Every important finding maps to one clear action — for example, no immediate action, continue routine screening, start screening, begin earlier screening, increase frequency, obtain a confirmatory test, see a genetic counsellor or specialist, complete a diagnostic investigation, implement a prevention intervention, or review at your annual reassessment.
No result is returned without explaining what happens next.