Agent-native genomics
Your DNA, decoded into
things you can actually do
AI agents research every genetic variant in depth, cross-reference gene interactions, and distill it all into concrete actions — supplements, diet changes, lifestyle tweaks, things to monitor — personalized to your genotype.
Specific enough to act on
Not “you may have an increased risk.” Every recommendation names the genes behind it, the evidence level, and exactly what to do.
Use methylfolate instead of folic acid
MTHFR C677T · established evidence
400–800 mcg L-methylfolate daily. Your MTHFR enzyme converts folate at 30% efficiency — synthetic folic acid can't keep up.
Avoid fluoropyrimidine chemotherapy
DPYD D949V · established evidence
Severely reduced DPD enzyme activity. Standard doses of 5-FU or capecitabine could be life-threatening — alternative regimens required.
Build training around endurance
ACTN3 + PPARA · moderate evidence
No alpha-actinin-3 plus full PPARA fat oxidation. Your fast-twitch fibers are shifted aerobic — distance events are where your genetics give you the edge.
Genes don't work alone. Neither do we.
Most genetic services give you a list of isolated SNP factoids. GeneOps maps 273 gene-gene interactions that only activate when you carry a specific combination — not just one or the other.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
No specific gene interaction for this genotype combination.
Invest heavily in injury prevention Moderate
Stiffer connective tissue plus alpha-actinin-3 deficiency create compounded injury susceptibility — dedicated prehabilitation is essential.
COL5A1
ACTN3
Frontier AI models, rigorous methodology
Every article, recommendation, and gene interaction in GeneOps is produced by state-of-the-art research agents using the most capable models available — then validated against strict schemas before anything reaches users.
Deep per-variant research
A dedicated agent per SNP searches clinical databases, reads published studies, verifies allele orientations against dbSNP, and synthesizes findings with evidence-graded recommendations and PubMed citations.
Structured and queryable
All output is validated against strict schemas — genotype alleles, evidence levels, action types, citations — and loaded into a relational database where every fact is cross-referenced and queryable.
Continuously expanding
New categories and variants are added through orchestrated batch research runs. When we add new research, you get notified — re-upload your file and your results update in seconds.
Talk to your data
Your genetic results aren't a static report. Ask questions, explore interactions, get context — with an AI agent that has full access to both your personal results and our entire knowledge base.
Built-in AI agent
Ask anything about your results in plain language. The agent sees your full genotype profile, all your action items, gene interactions, and the research articles behind every recommendation.
- “What should I know about my methylation results?”
- “Which of my variants affect how I metabolize caffeine?”
- “Summarize all my supplement recommendations in one list.”
MCP server — bring your own agent
We expose your health data and our knowledge base as MCP tools (Model Context Protocol) — the open standard for connecting AI agents to external data. Use Claude Code, ChatGPT, Cursor, your own custom agent, or any MCP-compatible client.
Your personal data
Genotype results, action items, risk factors, gene interaction insights
Full knowledge base
213 variants, 1,516 recommendations, research articles, PubMed links
Your agent gets the same data the built-in agent uses — structured, up-to-date, and ready to reason about.
9 health categories and counting
Every category covers the genetic variants that matter most, from drug metabolism to sleep patterns to cardiovascular risk.
Three steps to your action plan
Upload your 23andMe data
Export your raw data file from 23andMe and upload it. We match your genotypes against our knowledge base in seconds.
Get personalized insights
See which variants you carry across all 9 categories, with severity flags and gene interactions automatically resolved.
Act on it
Get a concrete checklist of supplements, diet changes, tests to request, and things to avoid. Talk to your AI agent about any of it.
Start free, upgrade when you're ready
Upload your genome and explore your results at no cost. Unlock the full action plan for $99.
Free
No credit card required
- Upload and process your genome
- Dashboard with all category profiles
- Genotype results and explanations
- Browse the full knowledge base
- Preview action items (1 per category)
Lifetime
One-time. All future updates included.
- Everything in Free, plus:
- All action items — supplements, diet, lifestyle, monitoring
- Gene interactions and combined evidence
- Built-in AI agent for follow-up questions
- MCP API for your own AI agents
- Partner invitation for offspring analysis
Not ready to upload? The entire knowledge base is free to browse.
Explore 213 genetic variantsEvidence-graded
Every recommendation includes its evidence level. No hype, no overselling.
Not a diagnostic tool
Health intelligence for informed conversations with your doctor, not a replacement.