ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.1146C>A (p.Ile382=)

gnomAD frequency: 0.00001  dbSNP: rs185723423
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001458840 SCV001662669 likely benign Spinocerebellar ataxia type 19/22 2020-04-24 criteria provided, single submitter clinical testing
Ambry Genetics RCV003160860 SCV003854559 likely benign Cardiovascular phenotype 2023-02-15 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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