ClinVar Miner

Submissions for variant NM_004320.6(ATP2A1):c.2744+10C>T

gnomAD frequency: 0.00001  dbSNP: rs778200749
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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 RCV002145038 SCV002414966 likely benign Brody myopathy 2023-11-02 criteria provided, single submitter clinical testing

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