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).


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.

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We are pleased to announce that our manuscript has been published in Nucleic Acids Research. Please take a moment to check out our work in this prestigious journal.

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