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dbSNP VCF for BQSR

We are planing to work on GRCh38, and BQSR requires dbSNP VCF as input.
The latest one is v146 in GRCh38 here
ftp://ftp.ncbi.nlm.nih.gov/snp/organisms/human_9606_b146_GRCh38p2/VCF/

There are two files in dbSNP, one is ALL_20151104.vcf (3.2G) and another is common_all_20151104.vcf (0.9G). Which one should we use? Should we just take the file as is, or do we need some filtering (say MAF, multiallielic SNP, etc)

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