ClinVar Miner

Submissions for variant NM_138477.4(CDAN1):c.3119G>A (p.Gly1040Glu)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003144743 SCV003829428 uncertain significance Anemia, congenital dyserythropoietic, type 1a 2022-01-24 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV003481458 SCV004227369 uncertain significance not provided 2022-12-30 criteria provided, single submitter clinical testing PM2

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