List of variants in gene MT-ATP6 reported as likely pathogenic

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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ATP6):m.8719G>A	rs28624611
NC_012920.1(MT-ATP6):m.8783G>A	rs1603221804
NC_012920.1(MT-ATP6):m.9032T>C	rs1603221994
NC_012920.1(MT-ATP6):m.9035T>C	rs1603222000
NC_012920.1(MT-ATP6):m.9049G>A	rs1603222011
NC_012920.1(MT-ATP6):m.9134A>G	rs1603222119
NC_012920.1(MT-ATP6):m.9155A>G
NC_012920.1:m.8851T>C	rs199476136
NC_012920.1:m.8950G>A	rs1556423574
NC_012920.1:m.8969G>A	rs794726857
NC_012920.1:m.9166T>C	rs1057516063
NC_012920.1:m.9176T>C	rs199476135
NC_012920.1:m.9176T>G	rs199476135
NC_012920.1:m.9185T>C	rs199476138
NC_012920.1:m.9191T>C	rs1556423632

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.