ClinVar Miner

Submissions for variant NM_004408.4(DNM1):c.2430G>C (p.Gly810=)

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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 RCV003753548 SCV004390093 likely benign Developmental and epileptic encephalopathy, 31A 2024-09-09 criteria provided, single submitter clinical testing

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