ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.640-18C>T

gnomAD frequency: 0.00001  dbSNP: rs776778917
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003748352 SCV004524844 likely benign Hypertrophic cardiomyopathy 2023-10-13 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700942 SCV001921034 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702981 SCV001930126 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001702981 SCV001966626 likely benign not provided no assertion criteria provided clinical testing

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