ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.-17-13C>T

gnomAD frequency: 0.00003  dbSNP: rs545560860
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000331364 SCV000395407 uncertain significance Familial thoracic aortic aneurysm and aortic dissection 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001705475 SCV000729151 likely benign not provided 2020-04-17 criteria provided, single submitter clinical testing

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