ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.3001C>A (p.Arg1001=)

dbSNP: rs1064795023
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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 RCV001805288 SCV002052144 likely benign Familial thoracic aortic aneurysm and aortic dissection 2021-03-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002541425 SCV003308370 likely benign Aortic aneurysm, familial thoracic 4 2022-02-21 criteria provided, single submitter clinical testing

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