List of variants in gene MT-ND2 reported by ClinGen Mitochondrial Disease Nuclear and Mitochondrial Variant Curation Expert Panel, ClinGen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND2):m.4611del	rs1603219523
NC_012920.1(MT-ND2):m.4735C>G	rs1603219589
NC_012920.1(MT-ND2):m.4769A>G	rs3021086
NC_012920.1(MT-ND2):m.4810G>A	rs267606888
NC_012920.1(MT-ND2):m.4983C>T	rs1556422937
NC_012920.1(MT-ND2):m.5001dup	rs1603219713
NC_012920.1(MT-ND2):m.5133_5134del	rs199476116
NC_012920.1(MT-ND2):m.5293G>A	rs28690990
NC_012920.1(MT-ND2):m.5367_5385del	rs1603219920
m.5244G>A	rs199476115

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.