ClinVar Miner

Submissions for variant NM_001378969.1(KCND3):c.1518+18T>C

gnomAD frequency: 0.00001  dbSNP: rs377356478
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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 RCV002210117 SCV002365883 likely benign Spinocerebellar ataxia type 19/22 2025-01-22 criteria provided, single submitter clinical testing

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