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Table 7 Number of ATM submitted genetic variants

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

Submission significanceVariants
Uncertain significance2361
Likely benign1353
Pathogenic539
Benign135
Likely pathogenic312
Not provided48
Total4265
  1. Data available on the ClinVar Miner website: https://clinvarminer.genetics.utah.edu/. If a variant has more than one submission, it may be counted in more than one significance column. In this case, the total number of variants will be less than the total of the other cells.