ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.132C>T (p.Gly44=)

dbSNP: rs973818233
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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 RCV002200989 SCV002485670 likely benign Aortic aneurysm, familial thoracic 4 2024-10-10 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003528356 SCV004359489 likely benign Familial thoracic aortic aneurysm and aortic dissection 2022-03-02 criteria provided, single submitter clinical testing

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