Your data was sold and you weren't even in the room.
Know your magnitude
Upload your genetic data. See what the research actually says about your variants. Raw evidence, no spin, no prescriptions, and no one profiting from your biology but you.
Expressive is building the infrastructure for humanity to own its biology.
Today that means giving people a clear, honest picture of what their genome actually says. No hype, no prescriptions, just evidence.
Tomorrow it means a verifiable, privacy-preserving layer where your genetic and biological data can work for you. Funding research you believe in. Earning passive income from studies that need your profile. Proving things about yourself without revealing anything you didn't choose to share.
The endgame is a protocol, not a company. A genomic commons governed by the people in it, where researchers pay contributors directly, where your presence online earns you money through a zero-knowledge proof instead of making someone else rich, and where the platform is owned by its users because it literally cannot exist without them.
The deal has always been broken. We're fixing it.
Genetic health, clearly expressed
Every variant, explained
Search any rsID and find what the current research says: effect sizes, study quality, population data. No translation. Raw magnitude scores.
Research that updates
When new studies publish on your variants, you know. Not a one-time report. A living profile that grows with the science.
Upload once, query forever
23andMe, AncestryDNA, MyHeritage, Sequencing.com. Upload your raw data export. We extract your variants, encrypt them at rest, and immediately discard the original file. Your genetic data is never shared with third parties, never sold, and never used to train models.
How it works
- 1Upload your raw DNA file , processed immediately, raw file permanently discarded.
- 2We index your variants against 1.2 billion SNPs from GWAS Catalog, ClinVar, and dbSNP. Every finding is anchored to a real study , evidence tier and magnitude always visible.
- 3Your personalized report, live and updated as the research evolves. Filter by category, magnitude, or sentiment. Dive into citations. No paywalled conclusions.
Read the research. Then upload your file.
Every variant page is a plain-English summary of the published research, with PMID-linked citations and explicit hedging on weak evidence. We've indexed thousands of high-impact SNPs and genes , search a name you know or follow the catalog index.
Per-variant pages organized by gene and topic. Try rs4680 (COMT, dopamine breakdown) or rs1815739 (ACTN3, sprint vs endurance).
Per-gene summaries linking every variant we've indexed in that gene. Useful when you've heard of the gene before the rsID , APOE, MTHFR, BRCA1, etc.
23andMe sold. We won't.
In 2025, 23andMe sold its user data to TTAM Research Institute. You probably weren't notified. That's the industry you're used to. Here's how we're different , and why the architecture makes it provable.
Raw file discarded
Your original file is processed in memory and permanently deleted. We never store your raw genetic file , only the normalized variant data extracted from it.
Encrypted at rest and in transit
All genetic data is encrypted with AES-256. Your identity and your genome are held in separate encrypted databases , never linked in plain text.
Never sold. Never shared.
Your genetic data is not a product. We don't share it with insurers, employers, pharmaceutical companies, or research institutions without your explicit consent. When you consent, you choose the terms.
Built to HIPAA standards
Access controls, audit logs, encrypted storage, and breach notification procedures , built in from day one, not bolted on later.
Your biology should work for you.
Earn from your data. Opt in to research studies that match your genetic profile. Researchers pay contributors directly. You set the terms, you see the study, you decide.
Prove things without revealing them. Zero-knowledge proofs let you verify facts about your genome , to insurers, employers, researchers , without exposing the underlying data. Your proof. Your call.
Own the platform. The endgame is a protocol governed by the people in it. Not a company that can be acquired, pivoted, or sold. A commons that belongs to its contributors because it cannot exist without them.
We don't prescribe. We describe.
Evidence quality is always visible. If the research is weak, we say so. If something doesn't have mechanistic backing, it's not in your report.
Your genome is the most intimate data you own. You should be the one deciding who sees it, what they learn from it, and whether they pay for the privilege.
Get notified about early access
Drop your email and we'll let you know the moment access opens. We're working through the waitlist as fast as the corpus grows.
No spam. No wellness washing. Your genetic data stays yours.