ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.492+14T>C

dbSNP: rs1057523132
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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 RCV001180435 SCV001345368 likely benign Hereditary cancer-predisposing syndrome 2019-04-22 criteria provided, single submitter clinical testing
Invitae RCV002560802 SCV003460386 likely benign PTEN hamartoma tumor syndrome 2021-11-26 criteria provided, single submitter clinical testing

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