List of variants in gene MT-TY reported as uncertain significance for congenital myopathy

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TY):m.5837G>A	rs1603220147
NC_012920.1(MT-TY):m.5840C>A	rs1603220149
NC_012920.1(MT-TY):m.5841T>C	rs1603220150
NC_012920.1(MT-TY):m.5852T>C	rs1603220153
NC_012920.1(MT-TY):m.5858T>C	rs1603220157
NC_012920.1(MT-TY):m.5864G>A	rs1603220158
NC_012920.1(MT-TY):m.5865T>C	rs1603220159
NC_012920.1(MT-TY):m.5885T>C	rs1603220164
NC_012920.1(MT-TY):m.5889A>G	rs1603220167

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.