ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.741C>T (p.Arg247=)

dbSNP: rs2151299059
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001525918 SCV001736125 likely benign Familial thoracic aortic aneurysm and aortic dissection 2021-02-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002568116 SCV003299923 likely benign Aortic aneurysm, familial thoracic 4 2022-03-29 criteria provided, single submitter clinical testing

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