Genomics · Database
MyVariant.info
A variant annotation service that aggregates dbSNP, ClinVar, gnomAD, CIViC, snpEff and other sources by HGVS identifier.
What MyVariant.info is
A variant annotation service that aggregates dbSNP, ClinVar, gnomAD, CIViC, snpEff and other sources by HGVS identifier.
Query it here
The research agent queries MyVariant.info directly — no account, no API key — and every answer links back to the record it came from. Ask in plain language and it writes the query.
Questions
Can I search MyVariant.info without writing code?
Yes. The research agent queries MyVariant.info directly, with no account or API key, and cites the record behind every answer. Ask in plain language — for a gene, a protein, a compound or a study — and it builds the query for you.
Can I reuse data from MyVariant.info?
Aggregator: each block carries its source's licence (_license); TSRI terms of use. Only blocks whose licence allows reuse are kept (dbSNP, ClinVar, gnomAD and ExAC, CIViC, ClinGen, UniProt, snpEff, GWAS Catalog); CADD, dbNSFP, COSMIC, CGI, SNPedia and blocks with no stated licence are removed here. Terms: https://myvariant.info/terms/