ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.1462-13T>C

gnomAD frequency: 0.00001  dbSNP: rs766769240
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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 RCV002071793 SCV002426338 likely benign Spinocerebellar ataxia type 19/22 2023-10-03 criteria provided, single submitter clinical testing

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