ClinVar Miner

Submissions for variant NM_012281.3(KCND2):c.1115+13A>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 RCV002617265 SCV002958157 likely benign Early myoclonic encephalopathy 2023-10-13 criteria provided, single submitter clinical testing

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