ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.573C>A (p.Val191=)

dbSNP: rs763981310
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002171187 SCV002429354 likely benign Aortic aneurysm, familial thoracic 4 2022-09-26 criteria provided, single submitter clinical testing

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