ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.1372-6dup

dbSNP: rs769051410
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000994071 SCV002008401 likely benign not provided 2021-09-20 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 26582918)
Labcorp Genetics (formerly Invitae), Labcorp RCV002068717 SCV002446328 benign Spinocerebellar ataxia type 19/22 2022-08-31 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001701280 SCV001921370 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000994071 SCV001966450 likely benign not provided no assertion criteria provided clinical testing

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