ClinVar Miner

Submissions for variant NM_001321075.3(DLG4):c.210+2del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Service de Génétique Moléculaire, Hôpital Robert Debré RCV001270405 SCV001450690 likely pathogenic Intellectual developmental disorder 62 2020-06-09 no assertion criteria provided clinical testing

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