ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.3858+14G>A

dbSNP: rs71376096
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002152653 SCV002415475 likely benign Aortic aneurysm, familial thoracic 4 2025-01-26 criteria provided, single submitter clinical testing

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