ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.4776G>A (p.Arg1592=)

dbSNP: rs1242667613
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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 RCV002176292 SCV002479082 likely benign Aortic aneurysm, familial thoracic 4 2021-06-05 criteria provided, single submitter clinical testing

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