I just started using the package, but I notice that the documentation of ncbi_snp_query says that the function adds 1 to the positions of SNVs to match dbSNP. However, for indels (delins) it seems that the output position is off by 1 if you compare to the dbSNP page for the variant.
For example, compare the output below with dbSNP's website:
Hi, thanks for developing rsnps.
I just started using the package, but I notice that the documentation of
ncbi_snp_query
says that the function adds 1 to the positions of SNVs to match dbSNP. However, for indels (delins) it seems that the output position is off by 1 if you compare to the dbSNP page for the variant.For example, compare the output below with dbSNP's website:
https://www.ncbi.nlm.nih.gov/snp/?term=rs58275821