ClinVar Miner

Submissions for variant NM_018006.4(TRMU):c.-190A>T

gnomAD frequency: 0.00004  dbSNP: rs538113553
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
Illumina Laboratory Services, Illumina RCV000394619 SCV000439098 uncertain significance Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins 2016-06-14 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.