ClinVar Miner

Submissions for variant NM_138477.4(CDAN1):c.779A>G (p.Lys260Arg)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003144729 SCV003829407 uncertain significance Anemia, congenital dyserythropoietic, type 1a 2022-12-06 criteria provided, single submitter clinical testing

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