ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.4662G>A (p.Gln1554=)

dbSNP: rs2148511200
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002561974 SCV001678182 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2020-07-20 criteria provided, single submitter clinical testing
GeneDx RCV001638095 SCV001852650 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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