ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.2967C>G (p.Val989=)

dbSNP: rs1567717006
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, Inc, Center for Human Genetics, Inc RCV000680557 SCV000807970 likely benign Connective tissue disorder 2018-06-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004004222 SCV004840310 likely benign Familial thoracic aortic aneurysm and aortic dissection 2023-12-13 criteria provided, single submitter clinical testing

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