ClinVar Miner

Submissions for variant NM_006950.3(SYN1):c.378-19T>A

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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 RCV002598860 SCV003489738 likely benign Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders 2024-12-24 criteria provided, single submitter clinical testing

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