ClinVar Miner

Submissions for variant NM_016599.5(MYOZ2):c.*4G>T

dbSNP: rs1561137822
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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 RCV000770203 SCV000901631 uncertain significance Cardiomyopathy 2017-04-03 criteria provided, single submitter clinical testing

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