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Endpoint · lookupGETsaylorinnovations.com/api/bio/variant/rs334

Genetic Variant Clinical Significance (ClinVar).
Read moreGenetic Variant Clinical Significance (ClinVar). Genetic variant clinical significance from ClinVar by rsID, ClinVar id (VCV) or HGVS: pathogenic / benign / uncertain classification, review status with 0-4 stars, conditions, genes, molecular consequence, protein change and last evaluated date, best-reviewed record first. NCBI ClinVar, public domain; not medical advice.
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UNRATED
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7lsjfrjf8f…yuvxacy7
URL
https://saylorinnovations.com/api/bio/variant/rs334
MCP server on this host: com.saylorinnovations/data
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first 8 days ago · last 10 hr ago
12 free handshakes

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Polygon, Arbitrum, Base, Solana USDC
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Verify it yourselfnpx teppi-check https://saylorinnovations.com/api/bio/variant/rs334curl -s https://api.teppi.xyz/v1/trust/cap_01M3E3X0RMASZPDY9P86NQCKT7