ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.3048A>G (p.Ala1016=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003087711 SCV003472900 likely benign Aortic aneurysm, familial thoracic 4 2022-10-13 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004808418 SCV005430606 likely benign Familial thoracic aortic aneurysm and aortic dissection 2024-04-16 criteria provided, single submitter clinical testing

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