ClinVar Miner

Submissions for variant NM_000256.3(MYBPC3):c.2382G>A (p.Pro794=)

dbSNP: rs1565625459
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000774201 SCV000907902 likely benign Cardiomyopathy 2018-10-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000938779 SCV001084602 likely benign Hypertrophic cardiomyopathy 2024-12-02 criteria provided, single submitter clinical testing

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