ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.10495-10T>C

gnomAD frequency: 0.00003  dbSNP: rs750850264
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001180105 SCV001344964 benign Cardiomyopathy 2019-12-04 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002560797 SCV001688545 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2024-07-11 criteria provided, single submitter clinical testing

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