I was hoping to find someone with some experience of human variation databases.
How long will it take for the SNPs discovered in the 1000 genome project to make their way into public databases like dbSNP?
Which human variation database has the best coverage of SNPs. Will all of the SNPs in dbSNP be covered in HGMD and vice versa?
Which database is the 'best' if you are interested in investigating SNPs in a clinical context?
Are there any pros/cons of the different databases (dnSNP/HGVbase/HGMD)