List of variants in gene MT-ND2 reported as benign for Leigh syndrome

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: 51

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND2):m.4491G>A	rs201172504
NC_012920.1(MT-ND2):m.4501C>T	rs1603219484
NC_012920.1(MT-ND2):m.4506A>G	rs11510099
NC_012920.1(MT-ND2):m.4512G>A	rs1603219492
NC_012920.1(MT-ND2):m.4560G>A	rs1603219511
NC_012920.1(MT-ND2):m.4561T>C	rs41376350
NC_012920.1(MT-ND2):m.4596G>A	rs1117207
NC_012920.1(MT-ND2):m.4615A>G	rs386828946
NC_012920.1(MT-ND2):m.4639T>C	rs41510547
NC_012920.1(MT-ND2):m.4659G>A	rs1556422882
NC_012920.1(MT-ND2):m.4674A>G	rs1556422884
NC_012920.1(MT-ND2):m.4695T>C	rs1556422885
NC_012920.1(MT-ND2):m.4696T>C	rs1603219566
NC_012920.1(MT-ND2):m.4705T>C	rs1603219572
NC_012920.1(MT-ND2):m.4707C>T	rs1603219574
NC_012920.1(MT-ND2):m.4722A>G	rs1569483952
NC_012920.1(MT-ND2):m.4732A>G	rs201854167
NC_012920.1(MT-ND2):m.4734A>G	rs1603219588
NC_012920.1(MT-ND2):m.4735C>A	rs1603219589
NC_012920.1(MT-ND2):m.4767A>G	rs1569483957
NC_012920.1(MT-ND2):m.4824A>G	rs1556422903
NC_012920.1(MT-ND2):m.4833A>G	rs386419995
NC_012920.1(MT-ND2):m.4843C>T	rs1556422913
NC_012920.1(MT-ND2):m.4924G>A	rs386828956
NC_012920.1(MT-ND2):m.4936C>T	rs1603219679
NC_012920.1(MT-ND2):m.4959G>A	rs1603219694
NC_012920.1(MT-ND2):m.4960C>T	rs1603219696
NC_012920.1(MT-ND2):m.4965A>G	rs879150535
NC_012920.1(MT-ND2):m.5046G>A	rs878927053
NC_012920.1(MT-ND2):m.5074T>C	rs1556422946
NC_012920.1(MT-ND2):m.5076C>T	rs386828960
NC_012920.1(MT-ND2):m.5178C>A	rs28357984
NC_012920.1(MT-ND2):m.5186A>T	rs878939965
NC_012920.1(MT-ND2):m.5194C>T	rs1603219824
NC_012920.1(MT-ND2):m.5206C>T	rs1556422963
NC_012920.1(MT-ND2):m.5211C>T	rs1603219834
NC_012920.1(MT-ND2):m.5262G>A	rs1603219855
NC_012920.1(MT-ND2):m.5263C>T	rs41320049
NC_012920.1(MT-ND2):m.5277T>C	rs1556422968
NC_012920.1(MT-ND2):m.5301A>G	rs199794187
NC_012920.1(MT-ND2):m.5319A>G	rs28456039
NC_012920.1(MT-ND2):m.5331C>A	rs200778062
NC_012920.1(MT-ND2):m.5437C>T	rs1603219948
NC_012920.1(MT-ND2):m.5442T>C	rs3020601
NC_012920.1(MT-ND2):m.5460G>A	rs3021088
NC_012920.1(MT-ND2):m.5463C>T	rs1556422993
NC_012920.1(MT-ND2):m.5466A>G	rs1603219973
NC_012920.1(MT-ND2):m.5493T>C	rs1603219983
NC_012920.1:m.5302T>C	rs878853115
m.4640C>A	rs387906426
m.4917A>G	rs28357980

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.