Mental Health Medication+ Genetics Report

No. This is not a medical device, diagnostic test, or clinical service. This is an educational report that summarizes published pharmacogenomic research as it may relate to your genetic variants. It is not FDA-approved or clinically validated. It does not diagnose conditions, recommend treatments, or replace professional medical advice. Always consult a qualified healthcare provider before making any medication decisions.

Our report works with raw DNA data from 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, Living DNA, and most other consumer genetic testing services. Note that consumer DNA tests have limitations compared to clinical-grade pharmacogenomic testing and may not capture all relevant genetic variants.

Your complete DNA file is processed locally in your browser—your full genetic file is never uploaded to our servers. We extract and store only the specific genetic variants (~1,000 SNPs) needed for pharmacogenomic analysis. This extracted data is encrypted and stored securely. We never sell or share your genetic information with third parties.

Our report summarizes publicly available research from CPIC (Clinical Pharmacogenetics Implementation Consortium) guidelines, FDA drug labels, the PharmGKB database, and peer-reviewed pharmacogenomic studies. Each finding includes evidence tier ratings and citations. We present this research for educational purposes—interpretation and clinical application should be done by qualified healthcare professionals.

This is not a substitute for clinical pharmacogenomic testing. Clinical tests (like those ordered by physicians) are performed in CLIA-certified labs with validated methodologies and provide results intended for clinical decision-making. Our educational report uses consumer DNA data to help you understand published research—it is not clinically validated and should not be used to make medical decisions without consulting a healthcare provider.

Yes, you may share this report with your healthcare provider as a conversation starter. The report includes research citations that providers can review. However, your provider may recommend clinical-grade pharmacogenomic testing for validated results before making any treatment decisions. This report is educational and does not replace clinical testing.

Your report generates in seconds after uploading your DNA data. Since you already have the genetic data from a consumer testing service, we analyze it and present relevant research findings immediately.

Important limitations: (1) Consumer DNA tests may not detect all clinically relevant variants; (2) Pharmacogenomics is only one factor in medication response—other factors like age, weight, other medications, and health conditions also matter; (3) Research findings may not apply to all individuals; (4) This report is not FDA-approved or clinically validated; (5) New research may change current understanding. Always consult healthcare professionals for medical decisions.