Free where it should be free.
Paid where it costs us something.
Looking up what a gene means costs us nothing, so it costs you nothing. Parsing a genome or a lab report does, so that is what you pay for — never per seat, and never as a subscription to read your own users’ data.
€0
No key · No account · Stays free
Knowledge endpoints
GET /genes/{symbol} — function, variants, phenotypes, caveatsGET /variants/{rsid} — gene, alleles, effectGET /pgx/{gene}/{drug} — CPIC/DPWG guideline, phenotype groups, cited summarySources on every record
CORS-open, cacheable for an hour
OpenAPI 3.1 and
llms-full.txt€0
During the private beta · Access opened by hand · Not yet deployed
Parsing endpoints
POST /dna/parse — consumer exports, build stated (VCF later in the beta)POST /dna/annotate — ClinVar, PharmGKB, gnomAD, GWASPOST /bloodwork/parse — any lab PDF, lab’s own rangesPOST /crossover — predispositions read against the lab's own rangesZero retention by design
Data processing agreement before the first real file
After the beta, parsing is priced by usage, with a free tier that is real: enough to build and demo on, not a trial. Whether the unit is the file or the connected profile, and the number, are published before general availability, not sprung on beta partners. The knowledge endpoints stay free.
Educational, not diagnostic · Based in Spain, under Spanish and EU law · Zero retention by design · Data handling