ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.969T>C (p.Phe323=)

dbSNP: rs757012715
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002200006 SCV002357009 likely benign Spinocerebellar ataxia type 19/22 2021-11-20 criteria provided, single submitter clinical testing

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