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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.5592A>G	rs1603220042
NC_012920.1(MT-CYB):m.5601C>T	rs376884056
NC_012920.1(MT-CYB):m.5603C>T	rs369496446
NC_012920.1(MT-CYB):m.5605A>G	rs878963919
NC_012920.1(MT-CYB):m.5618T>C	rs1603220060
NC_012920.1(MT-CYB):m.5628T>C	rs1556423015
NC_012920.1(MT-CYB):m.5633C>T	rs879226228
NC_012920.1(MT-CYB):m.5655T>C	rs1556423019

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.