ClinVar Miner

Submissions for variant NM_003079.5(SMARCE1):c.423T>G (p.Ala141=)

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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 RCV002848299 SCV003233923 likely benign Familial meningioma 2023-07-10 criteria provided, single submitter clinical testing

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