ClinVar Miner

Submissions for variant NM_019074.4(DLL4):c.1844A>G (p.Tyr615Cys)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Cologne University RCV005054514 SCV005687795 uncertain significance Adams-Oliver syndrome 6 2024-11-25 criteria provided, single submitter clinical testing

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