ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.370-14del

dbSNP: rs1272403496
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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 RCV002142302 SCV002415182 likely benign Familial meningioma 2022-08-23 criteria provided, single submitter clinical testing

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