ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.894A>G (p.Gln298=)

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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 RCV002731549 SCV003018240 likely benign PTEN hamartoma tumor syndrome 2022-03-09 criteria provided, single submitter clinical testing

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