ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.519C>T (p.Phe173=)

gnomAD frequency: 0.00004  dbSNP: rs144600384
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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 RCV000863811 SCV001004529 likely benign Spinocerebellar ataxia type 19/22 2023-07-07 criteria provided, single submitter clinical testing
Ambry Genetics RCV004027603 SCV005023559 likely benign Cardiovascular phenotype 2023-12-12 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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