Open Shicheng-Guo opened 2 years ago
We plan to expand our coverage to include all variants in dbSNP and TOPMed, but it won't happen until next year. We don't have any plan to expand additional resources. My guess is most, if not all, SNPs from UKB and FinnGEN are included in the above resources.
Great. Thanks HuaiYu!!
dbSNP155 will be a good choice!!
Dear Team,
I am wondering How to handle SNPs which are not included in Haplotype Reference Consortium (HRC)? For example, rare/specific SNPs from UKB, FinnGEN, etc.
Thanks.
Shicheng