bio-clinical-databases-myvariant-queries

What problem does it solve?

Query myvariant.info API to retrieve aggregated variant annotations from ClinVar, gnomAD, dbSNP, COSMIC, and other data sources in a single request, simplifying multi-database annotation workflows.

Core Features & Use Cases

• Single-variant lookups and batched processing to fetch aggregated annotations (e.g., ClinVar, gnomAD, dbSNP, COSMIC)
• Flexible input formats: HGVS notation, rsID, or gene:protein notation
• Batch up to 1000 variants per request and parse nested responses into structured data for analysis
• Integrate into bioinformatics pipelines and downstream reporting for comparative annotation analyses

Quick Start

Query myvariant.info for a set of variants and retrieve aggregated annotations across ClinVar, gnomad, and dbSNP.