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URL: https://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg38&g=snp151
Proper Citation: dbSNP151 (RRID:SCR_028814)
Description: Database containing common germline alterations. dbSNP build 151 contains a subset of common germline variants (such as single nucleotide polymorphisms) defined by a minor allele frequency (MAF) of 1% or greater in major population groups.Database is used as a reference for various applications, such as measuring non-synonymous mutations in tumor mutation burden calculations.
Resource Type: data or information resource, database
Keywords: common germline alterations, subset of common germline variants, minor allele frequency,
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