ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.*578dup

dbSNP: rs113047070
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000346497 SCV000356537 uncertain significance Arrhythmogenic right ventricular cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000384764 SCV000356538 uncertain significance Catecholaminergic polymorphic ventricular tachycardia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001778887 SCV002015364 likely benign not provided 2021-05-15 criteria provided, single submitter clinical testing

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