ClinVar Miner

Submissions for variant NC_012920.1:m.11896C>G

dbSNP: rs1057516065
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Neuroscience and Cell Biology, University of Coimbra, Portugal RCV000408935 SCV000484523 uncertain significance Hearing impairment; Dyssynergia; Peripheral neuropathy 2016-11-21 no assertion criteria provided 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.