ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.14091-12_14091-11dup

dbSNP: rs35563566
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001647359 SCV001859314 benign not provided 2019-08-19 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799096 SCV002042899 benign Cardiomyopathy 2020-12-10 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001528461 SCV002766116 benign not specified 2022-11-28 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001528461 SCV001740251 benign not specified no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001528461 SCV001922038 benign not specified no assertion criteria provided clinical testing

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