ClinVar Miner

Submissions for variant NM_004320.6(ATP2A1):c.819T>G (p.Leu273=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002619932 SCV003504934 likely benign Brody myopathy 2024-02-02 criteria provided, single submitter clinical testing

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