ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.1308A>G (p.Leu436=)

dbSNP: rs2108400390
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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 RCV002078029 SCV002324272 likely benign Cowden syndrome 2021-02-21 criteria provided, single submitter clinical testing

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