ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.1249-15G>T

dbSNP: rs886051765
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000260251 SCV000395386 uncertain significance Familial thoracic aortic aneurysm and aortic dissection 2016-06-14 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000260251 SCV001343338 likely benign Familial thoracic aortic aneurysm and aortic dissection 2019-02-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005090470 SCV005751305 likely benign Aortic aneurysm, familial thoracic 4 2025-01-29 criteria provided, single submitter clinical testing

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