Interface to the g:Profiler tool g:SNPense that maps SNP rs identifiers to chromosome positions, genes and variant effects.
Available only for human SNPs.
Usage
gsnpense(query, filter_na = TRUE)
Arguments
query
vector of SNP IDs to be translated (should start with prefix 'rs').
filter_na
logical indicating whether to filter out results without a
corresponding target name.
Value
The output is a data.frame which is a table closely corresponding to the
web interface output. Columns 'ensgs' and 'gene_names' can contain list of multiple values.