ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.2410C>T (p.Leu804=)

gnomAD frequency: 0.00001  dbSNP: rs1169056407
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004009935 SCV004820327 likely benign Cardiomyopathy 2023-08-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005103216 SCV005775512 likely benign Hypertrophic cardiomyopathy 2024-03-06 criteria provided, single submitter clinical testing

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