domains / families / science / myvariant-queries

myvariant-queries

separate

Queries myvariant.info BioThings aggregator for ClinVar, gnomAD, dbSNP, dbNSFP, COSMIC, CADD, and CIViC annotations in batched, version-tracked requests. Use when annotating variant lists from multiple databases simultaneously without managing per-source APIs, and when reproducibility-grade analyses require recording source data versions via _meta.

When to use

• annotating variant lists from multiple databases simultaneously
• reproducibility-grade analyses requiring recording source data versions
• batched, version-tracked requests
• querying ClinVar, gnomAD, dbSNP, dbNSFP, COSMIC, CADD, and CIViC annotations
• single canonical-ID lookup
• batch lookup up to 1000 IDs
• flexible Elasticsearch search
• per-source version metadata retrieval

When not to use

• producing ACMG calls
• offline or PHI-sensitive analysis
• local annotation tool pipeline integration
• family or cohort analysis
• clinical lab ACMG criteria auto-application

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