List of variants in gene MT-TW reported as benign for MELAS syndrome

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: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TW):m.5514A>G	rs1603219997
NC_012920.1(MT-TW):m.5515A>G	rs1603220000
NC_012920.1(MT-TW):m.5527A>G	rs1603220005
NC_012920.1(MT-TW):m.5528T>C	rs1556423004
NC_012920.1(MT-TW):m.5530C>T	rs1603220009
NC_012920.1(MT-TW):m.5539A>G	rs1603220013
NC_012920.1(MT-TW):m.5553T>C	rs878853053
NC_012920.1(MT-TW):m.5554C>A	rs1603220020
NC_012920.1(MT-TW):m.5557T>C	rs1603220022
NC_012920.1(MT-TW):m.5558A>G	rs370471013
NC_012920.1(MT-TW):m.5563G>A	rs1603220027
NC_012920.1(MT-TW):m.5567T>C	rs1603220030
NC_012920.1(MT-TW):m.5568A>G	rs200719361

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.