ClinVar Miner

Submissions for variant NM_005618.4(DLL1):c.1610_1611insCTA (p.Glu537delinsAspTer)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002290200 SCV002579364 uncertain significance Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures 2021-06-22 criteria provided, single submitter clinical testing

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