ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.4366-4G>A

gnomAD frequency: 0.00001  dbSNP: rs760252350
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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 RCV001505768 SCV001710678 likely benign Aortic aneurysm, familial thoracic 4 2024-08-24 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001524817 SCV001734777 likely benign Familial thoracic aortic aneurysm and aortic dissection 2020-07-20 criteria provided, single submitter clinical testing

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