ClinVar Miner

Submissions for variant NM_004320.6(ATP2A1):c.2248G>A (p.Gly750Ser)

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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 RCV003486019 SCV004234570 uncertain significance Brody myopathy 2023-05-18 criteria provided, single submitter clinical testing

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