ClinVar Miner

Submissions for variant NM_138477.4(CDAN1):c.848C>G (p.Thr283Arg)

dbSNP: rs1168958842
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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 RCV002227320 SCV002506156 uncertain significance Anemia, congenital dyserythropoietic, type 1a 2021-12-19 criteria provided, single submitter clinical testing

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