ClinVar Miner

Submissions for variant NM_004320.6(ATP2A1):c.929-23_929-12del

dbSNP: rs551640234
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001762849 SCV001988779 benign not provided 2021-09-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073999 SCV002405216 benign Brody myopathy 2024-12-19 criteria provided, single submitter clinical testing

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