Hey PH 👋 Ben here, founder and solo dev of Expressive. A few years ago I uploaded my DNA to 23andMe expecting real answers. What I got back was a list of variants I had no idea what to do with. So I spent hundreds of hours manually digging through GWAS studies, ClinVar, PubMed, trying to piece together what my genetics actually meant for my health. One thing that actually changed my behavior: I found I carry risk variants associated with fatty liver disease. Got blood work done, AST and ALT were elevated for my age. Started making changes. Stuff I never would have acted on without going deep into the research myself. There was no platform that would just do this work. Evidence-weighted, kept current as research evolves, without monetizing your genome to pay the bills. So I built one. A few things that make Expressive different: Your raw file is encrypted on arrival, parsed, then discarded. We never sell it. Every finding is tied to a real source. GWAS Catalog, ClinVar, PharmGKB, PubMed. Not curated marketing content. Reports update automatically when new research lands on your variants. Beta is free and we support files from 23andMe, AncestryDNA, MyHeritage, Sequencing.com, and plain VCF. Would love your feedback, especially from anyone who has been sitting on a raw DNA file since the bankruptcy. Happy to answer anything about methodology, data sources, or architecture.

Expressive

Your raw DNA is finally useful for you

Your raw DNA is finally useful for you