ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.846C>T (p.His282=)

dbSNP: rs779250750
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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 RCV001403805 SCV001605690 likely benign Aortic aneurysm, familial thoracic 4 2018-10-31 criteria provided, single submitter clinical testing

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