ClinVar Miner

Submissions for variant NM_002180.2(IGHMBP2):c.87-19A>G (rs183650590)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000249860 SCV000308735 likely benign not specified criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001172584 SCV001335647 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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