ClinVar Miner

Submissions for variant NM_004320.6(ATP2A1):c.401G>A (p.Arg134His)

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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 RCV003143616 SCV003834347 uncertain significance Brody myopathy 2019-05-30 criteria provided, single submitter clinical testing

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