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Table 6 Number of submitted variants per significance

From: Variants of uncertain significance in the era of high-throughput genome sequencing: a lesson from breast and ovary cancers

Submission significanceVariantsGenes
Uncertain significance266,75913,346
Likely benign203,1419515
Benign128,36414,810
Pathogenic91,3229998
Likely pathogenic41,4044198
Not provided17,0661594
Other2134109
  1. Data available on the ClinVar Miner website: https://clinvarminer.genetics.utah.edu/