ClinVar Miner

List of variants in gene MT-TQ studied for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
Download table as spreadsheet
HGVS dbSNP
NC_012920.1(MT-CYB):m.4335C>T rs878959563
NC_012920.1(MT-CYB):m.4339G>A rs1603219415
NC_012920.1(MT-CYB):m.4340A>G rs1603219416
NC_012920.1(MT-CYB):m.4343A>G rs386828939
NC_012920.1(MT-CYB):m.4350C>T rs1603219418
NC_012920.1(MT-CYB):m.4353T>C rs1603219419
NC_012920.1(MT-CYB):m.4360G>A rs1603219422
NC_012920.1(MT-CYB):m.4370T>C rs1603219427
NC_012920.1(MT-CYB):m.4371T>C rs1603219428
NC_012920.1(MT-CYB):m.4372C>T rs1603219429
NC_012920.1(MT-CYB):m.4373T>C rs1603219432
NC_012920.1(MT-CYB):m.4375C>T rs1603219433
NC_012920.1(MT-CYB):m.4381A>G rs1603219434
NC_012920.1(MT-CYB):m.4384T>A rs1603219436
NC_012920.1(MT-CYB):m.4384T>C rs1603219436
NC_012920.1(MT-CYB):m.4385A>G rs386828941
NC_012920.1(MT-CYB):m.4385A>T rs386828941
NC_012920.1(MT-CYB):m.4386T>C rs1569483940
NC_012920.1(MT-CYB):m.4387C>T rs1556422854
NC_012920.1(MT-CYB):m.4394C>A rs1603219441
NC_012920.1(MT-CYB):m.4395A>G rs1603219443
NC_012920.1(MT-CYB):m.4399T>C rs1603219445
NC_012920.1(MT-CYB):m.4400A>G rs1603219449
NC_012920.1:m.4363T>C rs200009705
Single allele rs375986475
m.4332G>A rs199476141
m.4336T>C rs41456348

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.