ClinVar Miner

Submissions for variant NM_006218.4(PIK3CA):c.1959A>G (p.Leu653=)

dbSNP: rs1553823720
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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 RCV000631225 SCV000752239 likely benign Cowden syndrome 2017-11-02 criteria provided, single submitter clinical testing

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