ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2784G>A (p.Ser928=)

dbSNP: rs372510974
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000035526 SCV000059176 likely benign not specified 2010-04-09 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002504876 SCV002803119 likely benign Hypertrophic cardiomyopathy 4; Left ventricular noncompaction 10 2021-08-11 criteria provided, single submitter clinical testing
Invitae RCV003586130 SCV004280533 likely benign Hypertrophic cardiomyopathy 2023-04-09 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003531911 SCV004358664 likely benign Cardiomyopathy 2021-07-06 criteria provided, single submitter clinical testing

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