ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.6018T>C (p.His2006=)

dbSNP: rs757380341
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002536269 SCV001006180 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2023-10-14 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001524445 SCV001734291 likely benign Cardiomyopathy 2020-10-05 criteria provided, single submitter clinical testing

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