ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.370-16A>C

gnomAD frequency: 0.00002  dbSNP: rs773985049
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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 RCV002220375 SCV002363090 likely benign Familial meningioma 2023-11-24 criteria provided, single submitter clinical testing

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