ANNOVAR is a rapid, efficient tool to annotate functional consequences of genetic variation from high-throughput sequencing data. wANNOVAR provides easy and intuitive web-based access to the most popular functionalities of the ANNOVAR software
[5/9/2019] The wANNOVAR server is migrated to a new host. All submissions will be deleted within 1 day (new rule in June 2019) due to lack of storage space. Please download your results promptly.
[10/19/2017] The detailed amino acid changes for indels are now included in the output (through -polish argument in table_annovar). The server also handles duplicated entries (multiple identical variants) in the input file correctly.
[08/25/2017] The variants reduction method (for disease gene finding from personal genomes) has been updated to the latest version.
[07/31/2017] All databases are updated to 20170517 version.
[10/22/2015] Now the filter is working for hg38! However, the custom filter is not supported.
[07/16/2015] Now we added another select called 'Individual Analysis', which is designed for VCF files. If you want to include all the individuals in your VCF file, please choose 'All annotations'. If you want to conduct individual based analysis (the first one if multiple samples are present), please choose 'Individual analysis'.
The ANNOVAR software have been updated to the newest version! hg38 reference genome was added!
The Disease Model has been modified and now the 'rare recessive Mendelian disease' and 'rare dominant Mendelian disease' don't exclude SNPs in dbSNP database any more!