ClinVar Miner

List of variants in gene MT-TV reported as uncertain significance for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NC_012920.1(MT-CYB):m.1608G>A rs1603218582
NC_012920.1(MT-CYB):m.1619_1620insT rs1603218585
NC_012920.1(MT-CYB):m.1629A>G rs1603218587
NC_012920.1(MT-CYB):m.1631C>T rs1603218590
NC_012920.1(MT-CYB):m.1636A>G rs1603218591
NC_012920.1(MT-CYB):m.1638T>C rs1603218592
NC_012920.1(MT-CYB):m.1641G>A rs28416113
NC_012920.1(MT-CYB):m.1643A>G rs1603218595
NC_012920.1(MT-CYB):m.1654T>C rs1603218602
NC_012920.1(MT-CYB):m.1658T>C rs1603218607

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.