ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.531-15C>A

gnomAD frequency: 0.00001  dbSNP: rs559147441
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001178929 SCV001343494 likely benign Cardiomyopathy 2019-02-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003748318 SCV004518392 likely benign Hypertrophic cardiomyopathy 2023-02-19 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001178929 SCV004822220 likely benign Cardiomyopathy 2023-04-03 criteria provided, single submitter clinical testing

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