saylorinnovations.com
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, molecula
Go to this service →Our latest check (2026-10-11)
- Answering
- Yes — valid x402 payment terms
- Time to answer
- 354 ms
- Price
- $0.003 per call
- Paying buyers, last 30 days
- 1 (directory's own records)
- Paid calls, last 30 days
- 1
- Category
- Health (non-drug)
- Address
- https://saylorinnovations.com/api/bio/variant/:id
Accuracy
Accuracy scores are published once a seller has enough paid checks against an independent record (at least 7 scored answers over at least 7 days). Until then no score is shown, and a missing score is never a pass.
For agents
This page as JSON: /sellers/a0516e4bfa3c.json. Paid lookup by address: GET /api/seller?resource=… ($0.001, x402).