ClinVar Miner

Submissions for variant NM_003919.3(SGCE):c.912T>G (p.Pro304=)

dbSNP: rs1463065030
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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 RCV002113215 SCV002403016 likely benign Myoclonic dystonia 11 2021-08-24 criteria provided, single submitter clinical testing

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