Folklore Variant Evidence
Resolve and classify one public GRCh38 germline variant with Folklore.
Community: Submitted by a user or imported; check the owner before granting accessOnlineNo sign-inGlobalFreeRead-only
What it can do
- Search Variant Evidence: Classify, interpret or resolve one public GRCh38 germline SNV or simple indel smaller than 50 bp. Accepts coordinates, genomic/coding/protein HGVS, SPDI or rsID. Returns norma
What data it sees
Do you need an account
No: the server works without sign-in
Resolve and classify one public GRCh38 germline variant with Folklore. Accepts coordinates, genomic, coding and protein HGVS, SPDI and rsID; returns normalized identity, ACMG/AMP decision support, evidence, provenance and limitations for professional review.
Server tool list (1)
Raw names from tools/list. Only developers need these.
| search_variant_evidence | Classify, interpret or resolve one public GRCh38 germline SNV or simple indel smaller than 50 bp. Accepts coordinates, genomic/coding/protein HGVS, SPDI or rsID. Returns normalized variant identity, automated ACMG/AMP decision support, evidence, provenance and explicit limitations. This is variant-level decision support for professional review. It does not evaluate patient context and must not be presented as a diagnosis or treatment recommendation. Never choose a candidate when resolution is ambiguous. |