ClinVar Miner

Submissions for variant NM_001035.3(RYR2):c.8692A>G (p.Ile2898Val)

dbSNP: rs1558193694
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV000768776 SCV000900146 uncertain significance Cardiomyopathy 2017-07-31 criteria provided, single submitter clinical testing

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