ClinVar Miner

Submissions for variant NM_016599.5(MYOZ2):c.376+9T>A

gnomAD frequency: 0.00003  dbSNP: rs536009604
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV000770201 SCV000901629 uncertain significance Cardiomyopathy 2016-02-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001492541 SCV001697155 likely benign Hypertrophic cardiomyopathy 2024-12-22 criteria provided, single submitter clinical testing

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