Endpoint · lookupGETsaylorinnovations.com /api/bio/variant/rs334
Genetic Variant Clinical Significance (ClinVar).
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Genetic 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.Overview
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https://saylorinnovations.com/api/bio/variant/rs334
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npx teppi-check https://saylorinnovations.com/api/bio/variant/rs334curl -s https://api.teppi.xyz/v1/trust/cap_01M3E3X0RMASZPDY9P86NQCKT7