clinvar-annotation

SKILLWorkflowCommunity
v0.0.0ammawlaAGPL-3.0Aktualisiert vor 26 TQuelle →

Guide for annotating ENCODE regulatory variants with ClinVar clinical significance. Use when users need to check if variants in ENCODE peaks have clinical associations, find pathogenic variants in regulatory regions, or assess variant clinical impact. Trigger on: ClinVar, clinical significance, path

Community-submitted skill. Not yet reviewed by the Forge team. Full prompt content may not be available.Request review →
26Repo-Sterne
1Clients
1Formate
vor 26 TLetzte Aktualisierung
Skill
Autorammawla
Version0.0.0
LizenzAGPL-3.0
KategorieWorkflow
Formateskill.md
PromptNicht veröffentlicht
Kompatibilität
Claude✓ Unterstützt
Cursor
Copilot
ChatGPT
Gemini
Über

Guide for annotating ENCODE regulatory variants with ClinVar clinical significance. Use when users need to check if variants in ENCODE peaks have clinical associations, find pathogenic variants in regulatory regions, or assess variant clinical impact. Trigger on: ClinVar, clinical significance, pathogenic variant, variant classification, clinical variant, disease variant, VUS, benign, likely patho

Schlagwörter
skillclaude