ClinVar Miner

Submissions for variant NM_012281.3(KCND2):c.1044G>C (p.Gly348=)

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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 RCV002574263 SCV002931555 likely benign Early myoclonic encephalopathy 2025-02-02 criteria provided, single submitter clinical testing

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