ClinVar Miner

Submissions for variant NM_004320.6(ATP2A1):c.1765-4C>G

gnomAD frequency: 0.00001  dbSNP: rs757455246
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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 RCV000534304 SCV000638279 likely benign Brody myopathy 2025-02-03 criteria provided, single submitter clinical testing

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