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).
Start Exploring
or
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.