ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.156+10T>G

dbSNP: rs2037208869
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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 RCV001419255 SCV001621503 likely benign Familial meningioma 2023-03-08 criteria provided, single submitter clinical testing

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