ClinVar Miner

Submissions for variant NM_138477.4(CDAN1):c.1740-20C>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003764479 SCV004564315 likely benign Anemia, congenital dyserythropoietic, type 1a 2023-02-01 criteria provided, single submitter clinical testing

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