ClinVar Miner

Submissions for variant NM_012281.3(KCND2):c.1050G>A (p.Ser350=)

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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 RCV003070718 SCV003444152 likely benign Early myoclonic encephalopathy 2024-12-24 criteria provided, single submitter clinical testing

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