Know your risk. Understand what you can change.
Know what to do next.
GenomePramana is a precision-prevention platform — not a report portal. Share what we need, we rank your top health opportunities, you follow a measurable plan, we track whether it moved the number.
- 1UnderstandSignals from biomarkers, lifestyle and (optionally) genomic reports.
- 2PrioritiseTop 5 opportunities ranked by Impact × Modifiability × Evidence × Actionability × Readiness.
- 3InterveneEach opportunity ships with a baseline, objective and weekly actions.
- 4MeasureCheck-ins track adherence + biomarker shifts; outcomes attribute to interventions.
- 5LearnThe journey adapts — modify, escalate or declare win based on what moved.
Pick your doorway
You already have a genetic screening report (23andMe, Illumina, targeted panel). Upload it — we land it in counsellor review and still build your prevention map from your current labs.
No genomic test yet. Share current biomarkers, family history and lifestyle. We'll flag whether genomic testing would meaningfully add — without pushing unnecessary tests.
Start with your plate. Food logs + a biomarker check (fasting glucose, lipids) light up a nutrition-only pathway, no genomics required.
V1 ranks 8 opportunities across metabolic, cardio, activity, nutrition, recovery and screening — tuned for South Asian risk profiles. Hereditary cancer, pharmacogenomics, carrier screening and polygenic risk ship in subsequent phases.
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