ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.1514G>T (p.Gly505Val)

dbSNP: rs397516109
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Total submissions: 2
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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 RCV000770499 SCV000901944 uncertain significance Cardiomyopathy 2017-06-27 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000035728 SCV000059379 uncertain significance not specified 2009-01-02 no assertion criteria provided clinical testing

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