ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.528A>T (p.Leu176=) (rs1026599240)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000598349 SCV000704841 uncertain significance not provided 2016-12-27 criteria provided, single submitter clinical testing
Color RCV001178641 SCV001343144 likely benign Cardiomyopathy 2019-11-12 criteria provided, single submitter clinical testing

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