ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.8436+9T>G

gnomAD frequency: 0.00003  dbSNP: rs371760672
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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 RCV003033336 SCV002428247 likely benign Catecholaminergic polymorphic ventricular tachycardia 1 2025-01-27 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004526182 SCV005039467 likely benign not specified 2024-03-12 criteria provided, single submitter clinical testing

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