ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.873C>G (p.Ala291=)

dbSNP: rs2042214771
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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 RCV001479849 SCV001684155 likely benign Aortic aneurysm, familial thoracic 4 2023-07-25 criteria provided, single submitter clinical testing
Ambry Genetics RCV002377823 SCV002685835 likely benign Familial thoracic aortic aneurysm and aortic dissection 2019-07-26 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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