ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.4083C>T (p.Asn1361=)

dbSNP: rs769899465
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246734 SCV000306187 likely benign not specified criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001176605 SCV001340633 likely benign Familial thoracic aortic aneurysm and aortic dissection 2018-11-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001393023 SCV001594673 likely benign Aortic aneurysm, familial thoracic 4 2016-10-17 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001176605 SCV004821257 likely benign Familial thoracic aortic aneurysm and aortic dissection 2024-05-14 criteria provided, single submitter clinical testing

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