ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.492C>T (p.Ser164=)

dbSNP: rs1170371506
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001663483 SCV001879967 likely benign not specified 2020-12-23 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073092 SCV002468177 likely benign Spinocerebellar ataxia type 19/22 2021-10-15 criteria provided, single submitter clinical testing

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