Features
Eight ways to read your genome — built on peer-reviewed science.
Each feature is evidence-linked, reviewer-stamped, and accompanied by a clinical disclaimer.
DNA file upload + AI analysis
Upload raw data from 23andMe, AncestryDNA, MyHeritage, or FamilyTreeDNA. Free tier includes 5 baseline insights.
Personal health risk report
Genetic predisposition scores for 50+ conditions including cardiovascular, metabolic, neurological, and oncological markers.
Pharmacogenomics report
Drug compatibility table with metaboliser status, dosage notes, and an integrated halal-permissibility layer for users who request it.
Ancestry & trait prediction
Ethnic breakdown, migration paths, and physical and behavioural trait predictions.
Nutrition & fitness optimisation
Genome-informed diet, supplement, and training response guidance.
Rare disease identification
Variant flags cross-referenced with curated rare disease databases, with clear next-step counselor referral.
Find a genetic counselor
Searchable, verified directory filterable by country, specialty, and language.
AI genomics Q&A
Plain-English answers to genome questions, every response cites evidence and includes a clinical disclaimer.
Not medical advice. AI-generated insights are educational only. Always verify with a qualified healthcare professional.