ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.2619G>A (p.Leu873=)

dbSNP: rs771118861
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002195625 SCV002359742 likely benign Hypertrophic cardiomyopathy 2022-03-14 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004808201 SCV005431091 likely benign Cardiomyopathy 2024-05-14 criteria provided, single submitter clinical testing

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