ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.894A>G (p.Pro298=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003029105 SCV003326546 likely benign Cowden syndrome 2022-07-02 criteria provided, single submitter clinical testing

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