ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.634+9T>C

dbSNP: rs1589659798
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000913356 SCV001058501 likely benign PTEN hamartoma tumor syndrome 2021-12-23 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001180184 SCV001345052 likely benign Hereditary cancer-predisposing syndrome 2019-04-17 criteria provided, single submitter clinical testing

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