ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.816+7G>A

dbSNP: rs2143986787
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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 RCV001411175 SCV001613232 likely benign Familial meningioma 2020-08-24 criteria provided, single submitter clinical testing

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