Functional Annotation of Variants Online Resource
An open-access variant functional annotation portal for whole genome sequencing (WGS/WES) data. FAVOR contains total 8,892,915,237 variants (all possible 8,812,917,339 SNVs and 79,997,898 Observed indels).
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Announcing FAVOR-GPTFAVOR database and GPT-4 powered functional annotation interpretation
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With FAVOR's batch annotation feature, users can save time and effort by uploading a file with multiple variants or rsID to be annotated in batches, making it a valuable resource for researchers and clinicians working with WGS/WES data.