ClinVar Miner

Submissions for variant NM_001282684.2(KCTD17):c.906G>A (p.Glu302=)

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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 RCV002647763 SCV003523722 likely benign Myoclonic dystonia 26 2023-07-09 criteria provided, single submitter clinical testing

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