ClinVar Miner

Submissions for variant m.13708G>A

dbSNP: rs28359178
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
Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine RCV000854970 SCV000998017 benign Leigh syndrome 2019-10-17 criteria provided, single submitter clinical testing The NC_012920.1:m.13708G>A (YP_003024036.1:p.Ala458Thr) variant in MTND5 gene is interpretated to be a Benign variant based on the modified ACMG guidelines (unpublished). This variant meets the following evidence codes: BA1
OMIM RCV000010336 SCV000030562 pathogenic Leber optic atrophy 1992-09-30 no assertion criteria provided literature only
GeneReviews RCV000010336 SCV000087252 unknown Leber optic atrophy 2013-09-19 no assertion criteria provided curation Converted during submission to Uncertain significance.

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.