NCBI2R is a R package that annotates lists of SNPs and/or genes, with current information from NCBI, including LD information. Functions are provided that with one command will provide annotation of the results from genome wide association studies to provide a broader context of their meaning. Other functions enable comparisons between a user's GWA results, and candidate snp/gene lists that are created from keywords, such as specific diseases, phenotypes or gene ontology terms. Commands are simple to follow and designed to work with R objects to integrate into existing workflows. The output produces text fields and weblinks to more information for items such as: gene descriptions, nucleotide positions, OMIM, pathways, phenotypes, and lists of interacting and neighboring genes. Annotation can then be used in R for further analysis, or the objects can be customized for use in spreadsheet programs or web browsers. The NCBI2R package was designed to allow those performing genome analysis to produce output that could easily be understood by a person not familiar with R. Please see the new website at http://NCBI2R.wordpress.com for more information. The internet is required for almost all of these functions. Type PrintNCBI2RInfo() for information.