ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.2641C>T (p.Leu881=)

gnomAD frequency: 0.00002  dbSNP: rs907992794
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ClinVar version:
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 RCV001523976 SCV001733722 likely benign Cardiomyopathy 2020-07-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002568050 SCV002978102 likely benign Hypertrophic cardiomyopathy 2024-03-03 criteria provided, single submitter clinical testing

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