ClinVar Miner

List of variants reported as likely pathogenic for Leigh syndrome by Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_012920.1(MT-ATP6):m.8783G>A rs1603221804
NC_012920.1(MT-ATP6):m.9049G>A rs1603222011
NC_012920.1(MT-ATP6):m.9134A>G rs1603222119
NC_012920.1(MT-CO1):m.6526T>C rs1603220522
NC_012920.1(MT-ND2):m.4611del rs1603219523
NC_012920.1(MT-ND4):m.11621_11622del rs1603223363
NC_012920.1(MT-ND5):m.13063G>A rs1603224017
NC_012920.1:m.8851T>C rs199476136
m.12706T>C rs267606893
m.14453G>A rs199476107

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.