ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.36C>T (p.Ala12=)

dbSNP: rs2102000445
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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 RCV002185795 SCV002486115 likely benign Spinocerebellar ataxia type 19/22 2020-12-18 criteria provided, single submitter clinical testing

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