ClinVar Miner

Submissions for variant NM_012281.3(KCND2):c.1716-8del

dbSNP: rs570695615
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002127364 SCV002410721 benign Early myoclonic encephalopathy 2025-01-27 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004700632 SCV005204735 benign not specified 2024-06-17 criteria provided, single submitter clinical testing

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