ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.715-6T>G

gnomAD frequency: 0.00004  dbSNP: rs560583293
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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 RCV001351128 SCV001545568 likely benign Familial meningioma 2024-12-23 criteria provided, single submitter clinical testing

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