23andMe Analyzer

Upload your 23andMe raw data export to discover clinically significant genetic variants — matched against ClinVar and connected to the Crick knowledge base.

Privacy First

Your file is parsed entirely in-browser. Only variant IDs are sent for lookup — never your full genome.

ClinVar Powered

Variants are matched against NCBI ClinVar, the gold-standard database for clinical variant interpretation.

Connected Insights

Discovered genes link directly to Gene Decoder for disease associations, drug targets, and clinical trials.

Your data stays private

Your file is parsed in your browser. Only a filtered set of variant IDs (not your full genome) is sent to our server for ClinVar lookup. Nothing is stored.

Drop your 23andMe raw data file here

or click to browse. Accepts .txt files from 23andMe export.

Disclaimer: This tool is for educational and research purposes only. It is not a medical device and does not provide medical advice, diagnosis, or treatment. Genetic variant classifications are sourced from ClinVar and may change over time. Always consult a qualified healthcare professional or genetic counselor before making any health decisions based on genetic data.