ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.1106+10C>T

gnomAD frequency: 0.00016  dbSNP: rs377267051
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000712057 SCV000721726 likely benign not provided 2018-05-22 criteria provided, single submitter clinical testing
Athena Diagnostics RCV000712057 SCV000842471 benign not provided 2017-09-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001457195 SCV001660993 likely benign Spinocerebellar ataxia type 19/22 2023-12-11 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000610492 SCV001922258 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000712057 SCV001967872 likely benign not provided no assertion criteria provided clinical testing

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