Starting with a a few human single nucleotide polymorphisms (SNPs) how can I query a database of all known SNPS such that I can generate a list (data.table or csv file) of the 1000 or so closest SNPS, weather or not the SNP is a tagSNP, and what the minor allele frequency (MAF) is and how many bases it is away from the starting SNPS?
I would prefer to do this in R (although it does not have to be). Which database should I use? My only starting point would be listing the the starting snps (eg rs3091244 , rs6311, etc).
I am certain there is a nice simple Bioconductor package that could be my starting point. But what? Have you ever done it? I imagine it can be done in about 3 to 5 lines of code.