ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.4953+17G>A

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003740563 SCV004562743 likely benign not provided 2023-10-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV005063162 SCV005697291 likely benign Aortic aneurysm, familial thoracic 4 2024-06-22 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV005240917 SCV005888378 likely benign not specified 2025-01-04 criteria provided, single submitter clinical testing

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