ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.1028-7del

gnomAD frequency: 0.00001  dbSNP: rs750699769
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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 RCV001394063 SCV001595743 likely benign Familial meningioma 2024-01-03 criteria provided, single submitter clinical testing

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