ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.1A>G (p.Met1Val)

dbSNP: rs1555459260
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre for Genomic and Experimental Medicine, University of Edinburgh RCV000613766 SCV000731226 likely pathogenic Familial thoracic aortic aneurysm and aortic dissection no assertion criteria provided research

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