ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.3727-18C>T

gnomAD frequency: 0.00016  dbSNP: rs369549958
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001702980 SCV001940829 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002077148 SCV002423079 benign Hypertrophic cardiomyopathy 2025-01-20 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001700591 SCV005883635 likely benign not specified 2024-12-12 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700591 SCV001925069 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702980 SCV001929086 likely benign not provided no assertion criteria provided clinical testing

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