ClinVar Miner

Submissions for variant NM_000314.8(PTEN):c.635-11T>G

dbSNP: rs2132276315
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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 RCV002105678 SCV002401372 likely benign PTEN hamartoma tumor syndrome 2024-06-12 criteria provided, single submitter clinical testing

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