ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.522G>A (p.Glu174=)

dbSNP: rs2101997545
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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 RCV001443413 SCV001646383 likely benign Spinocerebellar ataxia type 19/22 2020-09-11 criteria provided, single submitter clinical testing

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