ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.156+15T>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003039184 SCV003333346 likely benign Familial meningioma 2022-12-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704877 SCV005212721 likely benign not provided criteria provided, single submitter not provided

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