ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.1960C>T (p.Leu654=)

dbSNP: rs1724929023
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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 RCV003754653 SCV004448185 likely benign Cowden syndrome 2023-03-18 criteria provided, single submitter clinical testing

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