ClinVar Miner

Submissions for variant NM_012281.3(KCND2):c.1375-7T>G

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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 RCV003599928 SCV004459387 likely benign Early myoclonic encephalopathy 2023-06-18 criteria provided, single submitter clinical testing

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