Turning an rs ID into a bioinformatics summary

Give it an rs ID. It pulls NCBI and Ensembl data, then writes a summary grounded in real PubMed citations instead of whatever Gemini remembers.

View source on GitHub

Enter an rs ID. The original app pulls variant data from NCBI and Ensembl, then asks Gemini to write a summary for bioinformaticians, grounded in real PubMed abstracts instead of the model's own recall. Below is that pipeline's real output for two example variants.

Fixed demo

Precomputed output for two example variants. No live API calls on this page. Try any rs ID in the real app ↗

Get a summary of a SNP given its rs ID

Shortcut links to the original record

NCBI Ensembl ClinVar