ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.165-7T>C

dbSNP: rs572375431
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000476308 SCV000554539 likely benign PTEN hamartoma tumor syndrome 2024-01-25 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000579739 SCV000686278 likely benign Hereditary cancer-predisposing syndrome 2016-09-23 criteria provided, single submitter clinical testing
GeneDx RCV001704563 SCV000728458 likely benign not provided 2020-07-16 criteria provided, single submitter clinical testing

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