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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
The text was updated successfully, but these errors were encountered:
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.
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
The text was updated successfully, but these errors were encountered: