ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.237+14A>T

gnomAD frequency: 0.00001  dbSNP: rs2037158156
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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 RCV002120802 SCV002440825 likely benign Familial meningioma 2021-03-17 criteria provided, single submitter clinical testing

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