From: Variants of uncertain significance in the era of high-throughput genome sequencing: a lesson from breast and ovary cancers
Submission significance
Variants
Genes
Uncertain significance
266,759
13,346
Likely benign
203,141
9515
Benign
128,364
14,810
Pathogenic
91,322
9998
Likely pathogenic
41,404
4198
Not provided
17,066
1594
Other
2134
109