ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1158-9_1173del

dbSNP: rs1651596554
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV001281579 SCV001468889 likely pathogenic Proximal muscle weakness no assertion criteria provided clinical testing

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