ClinVar Miner

Submissions for variant NM_004320.6(ATP2A1):c.1546-8T>C

dbSNP: rs2152211664
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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 RCV001440712 SCV001643623 likely benign Brody myopathy 2020-10-25 criteria provided, single submitter clinical testing

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