ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.4689G>A (p.Leu1563=) (rs770477774)

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Total submissions: 3
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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 RCV000769445 SCV000900838 uncertain significance Cardiomyopathy 2017-02-03 criteria provided, single submitter clinical testing
Color RCV000769445 SCV000904932 likely benign Cardiomyopathy 2018-09-18 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000275443 SCV000343296 uncertain significance not provided 2016-07-21 criteria provided, single submitter clinical testing

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