I would like to introduce a web-based variant annotation tool (http://jjwanglab.org/snvrap) which provides comprehensive local database of human genome variants with a user-friendly web page that provides a one-stop annotating service which is both convenient and up-to-date. A query can be accepted as either a dbSNP Id or a chromosomal location and web page instantly provide all the annotation information in an interactive LD panel. The system can also simultaneously prioritize this variant based on additive effect mode by corresponding annotation information and evaluate the variant effect that is then displayed in a prioritization tree.
It can act as a instant SNP annotation portal on web.