What If It's Not You?It Might Be Your Genes.
The average person tries 2-3 medications before finding one that works. Research suggests your genetics may influence how you process and respond to 110+ medications across mental health, cardiovascular, and pain. See your profile in minutes.
Choose Your Report:
"I built Brain Genome because I was tired of 'try this and see.' The research exists — you just couldn't access it."— Lindsey, Founder
Why Trial and Error Doesn't Work
Your genetics affect both how your body processes and how your brain responds to medications. Most prescribing doesn't account for either.
The Problem
2–3 medications over 12+ months. Each switch means more waiting, more side effects, more frustration.
Your Genetics
Gene variants can make standard doses build up too much (side effects) or clear too fast (doesn't work).
The Solution
Brain Genome shows how you process AND respond to 110+ medications across 3 reports — research-backed, in minutes.
A Smarter Starting Point
| Traditional | With Brain Genome |
|---|---|
| Try for 4–6 weeks, hope it works | See genetic insights in minutes |
| Switch if it doesn't work | See potential issues before you start |
| No idea why it's not working | Understand your processing + response |
| Months of trial and error | Research-backed starting point |
| Pay $300+ for clinical tests | Full insights for $19.95 |
110+ Medications Across 3 Reports
Your genetics may affect how you process medications across mental health, cardiovascular, and pain categories:
Start Free. Upgrade When Ready.
See your processing type for free. Full research for $19.95.
Free Report
- Your processing type for 110+ medications
- Fast, normal, or slow processor status
- All medication categories covered
Full Report
Everything in Free, plus:
- Metabolism pathway explanations
- Response & sensitivity factors
- Side effect susceptibility
- Drug interaction alerts
- Food, lifestyle & ancestry factors
- Evidence tiers & citations
- PDF download
Three Steps. That's It.
Upload DNA
Use existing 23andMe, AncestryDNA, or similar data.
Instant Analysis
Genetic variants analyzed in seconds — no waiting weeks.
Get Your Report
Processing type, research citations, and provider questions.
Transparent Research, Not a Black Box
Full Transparency
Evidence tiers and citations for every finding.
Privacy-First
DNA analyzed in your browser. We can't see it.
Research-Backed
CPIC guidelines, FDA labels, peer-reviewed sources.
Common Questions
Stop Guessing. Start Understanding.
See how you process 110+ medications using DNA you already have. Each report just $19.95.