ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.1129+8C>T

dbSNP: rs1355870460
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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 RCV000978165 SCV001126091 likely benign Aortic aneurysm, familial thoracic 4 2019-03-07 criteria provided, single submitter clinical testing

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