ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.14757-6C>T

gnomAD frequency: 0.00010  dbSNP: rs779122362
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000922641 SCV001068078 likely benign Catecholaminergic polymorphic ventricular tachycardia 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001619860 SCV001845927 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003150372 SCV003838732 likely benign Cardiomyopathy 2021-06-18 criteria provided, single submitter clinical testing

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