ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.370-8A>C

gnomAD frequency: 0.00001  dbSNP: rs368298445
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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 RCV001435792 SCV001638618 likely benign Familial meningioma 2018-12-15 criteria provided, single submitter clinical testing

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