ClinVar Miner

Submissions for variant NM_138477.4(CDAN1):c.2087T>A (p.Leu696Gln)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Emergency, The First Affiliated Hospital of Army Medical University RCV002280806 SCV002569069 pathogenic Anemia, congenital dyserythropoietic, type 1a no assertion criteria provided clinical testing

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