ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.79+14C>T

dbSNP: rs760610000
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001189902 SCV001357285 likely benign Hereditary cancer-predisposing syndrome 2019-08-22 criteria provided, single submitter clinical testing
Invitae RCV002069093 SCV002409891 likely benign PTEN hamartoma tumor syndrome 2021-11-22 criteria provided, single submitter clinical testing

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