List of variants in gene MT-TK 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: 10

Download table as spreadsheet

HGVS	dbSNP
NC_012920.1(MT-CYB):m.8308A>G	rs879081228
NC_012920.1(MT-CYB):m.8311T>C	rs371589230
NC_012920.1(MT-CYB):m.8337T>C	rs1603221405
NC_012920.1(MT-CYB):m.8343A>G	rs1603221411
NC_012920.1(MT-CYB):m.8345C>T	rs1603221413
NC_012920.1(MT-CYB):m.8347A>G	rs1603221417
NC_012920.1(MT-CYB):m.8348A>G	rs1556423430
NC_012920.1(MT-CYB):m.8349C>T	rs1603221418
NC_012920.1(MT-CYB):m.8360A>G	rs1603221422
m.8296A>G	rs118192102

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.