ClinVar Miner

Submissions for variant NM_002180.2(IGHMBP2):c.1714_1716del (p.Lys572del) (rs775542203)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Inherited Neuropathy Consortium RCV000789981 SCV000929370 uncertain significance Autosomal dominant distal hereditary motor neuropathy no assertion criteria provided literature only
Genesis Genome Database RCV000856974 SCV000999540 uncertain significance Charcot-Marie-Tooth disease 2019-08-14 no assertion criteria provided research

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.