ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.715-19G>A

gnomAD frequency: 0.00001  dbSNP: rs775623781
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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 RCV002185763 SCV002486106 likely benign Familial meningioma 2023-09-05 criteria provided, single submitter clinical testing

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