List of variants in gene MT-TR 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
NC_012920.1(MT-CYB):m.10410T>C	rs200478835
NC_012920.1(MT-CYB):m.10411A>G	rs1603222828
NC_012920.1(MT-CYB):m.10420A>G	rs1603222829
NC_012920.1(MT-CYB):m.10427G>A	rs1556423809
NC_012920.1(MT-CYB):m.10440T>C	rs1603222833
NC_012920.1(MT-CYB):m.10454T>C	rs878874133
NC_012920.1(MT-CYB):m.10455A>G	rs1603222840
NC_012920.1(MT-CYB):m.10463T>C	rs28358279

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.