ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.801+16T>C

dbSNP: rs2132277921
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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 RCV002126387 SCV002455232 likely benign PTEN hamartoma tumor syndrome 2024-09-27 criteria provided, single submitter clinical testing

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