ClinVar Database
For questions about ClinVar or data submission: clinvar@ncbi.nlm.nih.gov
LLM Evaluation
Evaluated by: xiaomi/mimo-v2-flash:free
Last evaluated: March 29, 2026
Prompt Preview
---
name: clinvar-database
description: Query NCBI ClinVar for variant clinical significance. Search by gene/position, interpret pathogenicity classifications, access via E-utilities API or FTP, annotate VCFs, for genomic medicine.
license: Unknown
metadata:
skill-author: K-Dense Inc.
---
# ClinVar Database
## Overview
ClinVar is NCBI's freely accessible archive of reports on relationships between human genetic variants and phenotypes, with supporting evidence. The database aggregates inf...
Full prompt length: 13228 characters
Tools & Technologies
- Python
- PostgreSQL
- MongoDB
- MySQL
- python