ClinVar Miner

Submissions for variant NM_001282684.2(KCTD17):c.-10G>A

gnomAD frequency: 0.00001  dbSNP: rs1924496959
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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 RCV002144481 SCV002461608 likely benign Myoclonic dystonia 26 2021-08-07 criteria provided, single submitter clinical testing

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