ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.1968+26A>G (rs80264244)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000508292 SCV000604107 benign not specified 2016-11-29 criteria provided, single submitter clinical testing
Epithelial Biology; Institute of Medical Biology, Singapore RCV000057378 SCV000088491 not provided not provided no assertion provided not provided
GeneDx RCV000057378 SCV000972283 benign not provided 2018-06-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.

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