ClinVar Miner

Submissions for variant NM_001353812.2(ATP11C):c.2114T>C (p.Ile705Thr)

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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 RCV003492925 SCV004234555 uncertain significance X-linked congenital hemolytic anemia 2023-02-27 criteria provided, single submitter clinical testing

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