ClinVar Miner

Submissions for variant NM_001353812.2(ATP11C):c.3063A>G (p.Ile1021Met)

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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 RCV003143595 SCV003832771 uncertain significance X-linked congenital hemolytic anemia 2022-08-18 criteria provided, single submitter clinical testing

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