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

Table 7 Number of ATM submitted genetic variants

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.

ISSN: 1756-9966