ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.2998-18_2998-17del

dbSNP: rs746744616
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002073411 SCV002432858 likely benign Aortic aneurysm, familial thoracic 4 2024-04-22 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001730197 SCV001977708 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001730197 SCV001978429 likely benign not provided no assertion criteria provided clinical testing

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