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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 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

  1. Data available on the ClinVar Miner website: https://clinvarminer.genetics.utah.edu/