SNPnexus is a web-based variant annotation tool designed to simplify and assist in the selection and prioritisation of known and novel genomic alterations. SNPnexus does not require any installation or registration and is free to use for everyone.
You can input the variants one by one or paste your query in the Text Area below.
Alternatively, you can upload a text file or vcf file with up to 100000 variants.
Please, refer to the User Guide for a detailed explanation of the input format.
Option 1 - Genomic Coordinates: