ClinVar Miner

Submissions for variant NM_002180.2(IGHMBP2):c.2612-14C>T (rs200940488)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000610962 SCV000716173 likely benign not specified 2017-02-28 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.
Molecular Genetics Laboratory,London Health Sciences Centre RCV001172587 SCV001335650 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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