ClinVar Miner

Submissions for variant NM_015074.3(KIF1B):c.3497C>T (p.Pro1166Leu) (rs141224290)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000197809 SCV000253528 benign Charcot-Marie-Tooth disease, type 2 2020-10-19 criteria provided, single submitter clinical testing
Vantari Genetics RCV000210783 SCV000267039 benign Hereditary cancer-predisposing syndrome 2015-12-07 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001172614 SCV001335677 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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.