ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1296_1299GCAC[4] (p.Ser437fs) (rs267607577)

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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 RCV000057266 SCV000188782 pathogenic not provided 2014-02-03 no assertion criteria provided clinical testing
Blueprint Genetics RCV000157296 SCV000207028 pathogenic Cardiomyopathy 2014-10-27 no assertion criteria provided clinical testing
Epithelial Biology; Institute of Medical Biology, Singapore RCV000057266 SCV000088379 not provided not provided no assertion provided not provided

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