ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.503-9T>C

dbSNP: rs969619157
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000937382 SCV000719933 likely benign not provided 2019-01-02 criteria provided, single submitter clinical testing
Invitae RCV001435468 SCV001638291 likely benign Hypertrophic cardiomyopathy 2021-11-23 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001526113 SCV001736398 likely benign Cardiomyopathy 2020-09-04 criteria provided, single submitter clinical testing

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