ClinVar Miner

Submissions for variant NM_003919.3(SGCE):c.463+19T>C

dbSNP: rs759488852
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002103618 SCV002395858 likely benign Myoclonic dystonia 11 2021-01-11 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004700619 SCV005203702 likely benign not specified 2024-07-03 criteria provided, single submitter clinical testing

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