ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.157-6T>C

gnomAD frequency: 0.00001  dbSNP: rs759579237
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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 RCV000878775 SCV001021739 likely benign Familial meningioma 2024-01-24 criteria provided, single submitter clinical testing

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