ClinVar Miner

List of variants in gene MT-TW reported as likely benign for Juvenile myopathy, encephalopathy, lactic acidosis AND stroke

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NC_012920.1(MT-CYB):m.5516A>G rs1603220001
NC_012920.1(MT-CYB):m.5539A>T rs1603220013
NC_012920.1(MT-CYB):m.5553T>G rs878853053
NC_012920.1(MT-CYB):m.5566A>G rs1603220029
NC_012920.1:m.5561T>C rs1556423009

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.