ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.1521G>A (p.Gly507=)

dbSNP: rs1235816440
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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 RCV001189796 SCV001357159 likely benign Cardiomyopathy 2019-04-28 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002491564 SCV002801878 likely benign Hypertrophic cardiomyopathy 4; Left ventricular noncompaction 10 2021-07-19 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004010381 SCV004834607 likely benign Hypertrophic cardiomyopathy 2023-03-28 criteria provided, single submitter clinical testing

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