ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.2667-20G>A

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003050868 SCV003444757 likely benign Cowden syndrome 2022-09-27 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003134599 SCV003808370 uncertain significance Cowden syndrome 5 2019-08-27 criteria provided, single submitter clinical testing

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