ClinVar Miner

Submissions for variant NM_006950.3(SYN1):c.528-12C>T

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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 RCV002614781 SCV003494610 likely benign Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders 2022-06-10 criteria provided, single submitter clinical testing

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