ClinVar Miner

Submissions for variant NM_138477.4(CDAN1):c.494C>T (p.Thr165Met)

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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 RCV003144739 SCV003829422 uncertain significance Anemia, congenital dyserythropoietic, type 1a 2022-12-21 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV003481457 SCV004227375 uncertain significance not provided 2022-11-30 criteria provided, single submitter clinical testing BP4, PM2

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