ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.1518+17A>C

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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 RCV003872619 SCV004686829 likely benign Spinocerebellar ataxia type 19/22 2023-06-27 criteria provided, single submitter clinical testing

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