ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1086del (p.Leu363fs) (rs58389804)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000143910 SCV000188781 pathogenic Primary dilated cardiomyopathy 2013-12-15 criteria provided, single submitter clinical testing
Blueprint Genetics RCV000057230 SCV000927815 pathogenic not provided 2018-07-20 criteria provided, single submitter clinical testing
Epithelial Biology; Institute of Medical Biology, Singapore RCV000057230 SCV000088343 not provided not provided no assertion provided not provided

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