ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.3293+7G>A

gnomAD frequency: 0.00001  dbSNP: rs201955317
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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 RCV000534548 SCV000641022 likely benign Aortic aneurysm, familial thoracic 4 2024-06-27 criteria provided, single submitter clinical testing

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