A curated set of health-relevant genetic markers — pharmacogenetic variants, classic carrier markers, common traits — explained in plain language with sources, confidence tiers, and population context. The lightweight, honest introduction. Educational, never diagnostic.
The Health & Traits report is a curated set of health-relevant genetic markers — pharmacogenetic variants, classic carrier markers, and common traits — presented with plain-language explanations, source citations, and appropriate caveats.
It's the lightweight introduction. If you want the full pipeline — pharmacogenetics split four ways, polygenic risk panels with population/N/year evidence, monogenic findings, longevity matching, modular cards with confidence tiers — that's the Health Studio subscription (€49.99/mo, separate product).
What this report is NOT: a diagnosis, a clinical service, a replacement for a doctor. Every result explicitly carries the educational, non-diagnostic framing. The point is calibrated reading of your genome's signal — not melodrama.
The full marker list ships with the report. Here's a representative sample of the kinds of variants you'll see.
Slow / fast metaboliser status. Affects how quickly caffeine clears your system.
TraitEuropean-type variant for adult lactose tolerance. Population-frequency context included.
PhenotypeReported with appropriate context. Population baseline framing, never alarmist headlines.
EducationCompanion to LCT. Together they explain dairy-tolerance status in adulthood.
TraitCommon variants with explained nuance — what's hype, what's actual evidence.
PGx-adjacentClassic hereditary hemochromatosis carrier markers, explained in plain language.
CarrierCommon variants with population-frequency notes; relevant for dietary & medication context.
CarrierDrug-metabolism variant. Sample marker — the full PGx pipeline lives in Health Studio.
PGxWhy some people taste broccoli as bitter and others don't. Lighter trait, well-studied.
TraitOne file, multiple reports. No second swab.
If your file lacks the SNP, the result is "not covered" — never silently filled.
Each marker gets evidence strength, population frequency, and the appropriate caveat.
Delivered to your dashboard with searchable cards plus an high-resolution image export.
Selected health-relevant variants with educational framing — pharmacogenetic, carrier, traits.
What's known, what's not, what the appropriate caveat is — for every marker.
If your raw file doesn't include the SNP, the report says "not covered" rather than inventing a result.
How common a variant is in your ancestry — context matters for interpretation.
Dashboard view with searchable cards. Filter, sort, drill in. Plus an high-resolution image export.
€6.36 lifetime. If you want the full pipeline (PGx, PRS, monogenic, carrier, longevity), upgrade to Health Studio.
Population baselines explained, evidence strength noted. The opposite of "you carry the gene for X" headlines.
Missing SNPs get flagged as "not covered" instead of being silently filled. Your raw file's actual content is respected.
When you want the full pipeline, Health Studio is right there — same upload, more depth, no surprise.
A lightweight introduction to your genome's health signal. If you want the full pipeline later, Health Studio is right there.