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SNPDelScore displays pre-compute deleterious effects of noncoding variants using a large panel of currently available methods and summarizes this information in an interactive, easy to use website. It also provides open access to these data through a RESTfull based web service and a Python based web services command line client to retrieve the data from other applications and tools.

Locus ID

SNP (rs62635286), gene name (DDX11L1) or genomic coordinates (chr8:11532494-11621567)