ClinVar Miner

Submissions for variant NM_004320.6(ATP2A1):c.324+7G>A

gnomAD frequency: 0.00001  dbSNP: rs373459786
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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 RCV000873771 SCV001015829 likely benign Brody myopathy 2024-09-14 criteria provided, single submitter clinical testing

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