ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.186G>C (p.Pro62=)

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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 RCV003640815 SCV004508613 likely benign Spinocerebellar ataxia type 19/22 2023-02-14 criteria provided, single submitter clinical testing

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