Hi everyone,
I have GWAS summary statistics with genetic variants (9M) and I want to obtain the rs that correspond to each of them. I have already download the VCF file of the whole dbSNP database but I do not know how to continue. I have already read the previous answers but they did not solve my problem. So in case anyone can help me I would be thankful. I am working with this type of data:
CHR SNP BP A1
1 chr1:732994:G:A 732994 A
1 chr1:758443:G:C 758443 C
1 chr1:794707:T:C 794707 C