ClinVar Miner

Submissions for variant NM_003919.3(SGCE):c.51A>G (p.Gly17=)

dbSNP: rs2117138100
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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 RCV001438783 SCV001641663 likely benign Myoclonic dystonia 11 2019-10-25 criteria provided, single submitter clinical testing

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