List of variants in gene MT-ND2 reported as uncertain significance 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: 61

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND2):m.4480T>C	rs1603219468
NC_012920.1(MT-ND2):m.4482G>A	rs1603219472
NC_012920.1(MT-ND2):m.4488C>T	rs1603219476
NC_012920.1(MT-ND2):m.4494A>G	rs1603219477
NC_012920.1(MT-ND2):m.4495T>C	rs1603219480
NC_012920.1(MT-ND2):m.4497T>C	rs1603219482
NC_012920.1(MT-ND2):m.4503A>T	rs1603219486
NC_012920.1(MT-ND2):m.4509T>C	rs1603219488
NC_012920.1(MT-ND2):m.4513C>T	rs1603219494
NC_012920.1(MT-ND2):m.4548T>C	rs1603219503
NC_012920.1(MT-ND2):m.4554A>G	rs1603219508
NC_012920.1(MT-ND2):m.4579T>C	rs1603219517
NC_012920.1(MT-ND2):m.4632G>A	rs1603219530
NC_012920.1(MT-ND2):m.4638A>G	rs878960801
NC_012920.1(MT-ND2):m.4659G>T	rs1556422882
NC_012920.1(MT-ND2):m.4665G>A	rs1603219544
NC_012920.1(MT-ND2):m.4676C>A	rs1603219551
NC_012920.1(MT-ND2):m.4680C>A	rs1603219554
NC_012920.1(MT-ND2):m.4690T>C	rs1603219557
NC_012920.1(MT-ND2):m.4717A>T	rs1603219578
NC_012920.1(MT-ND2):m.4745A>T	rs1556422896
NC_012920.1(MT-ND2):m.4746T>C	rs1603219594
NC_012920.1(MT-ND2):m.4749T>C	rs1603219596
NC_012920.1(MT-ND2):m.4759T>C	rs1603219604
NC_012920.1(MT-ND2):m.4764A>G	rs1603219609
NC_012920.1(MT-ND2):m.4765T>C	rs1603219611
NC_012920.1(MT-ND2):m.4768_4769delinsCG	rs1603219613
NC_012920.1(MT-ND2):m.4770G>A	rs1603219619
NC_012920.1(MT-ND2):m.4776G>A	rs1603219623
NC_012920.1(MT-ND2):m.4788G>A	rs1603219627
NC_012920.1(MT-ND2):m.4789G>A	rs1603219628
NC_012920.1(MT-ND2):m.4894T>C	rs1603219656
NC_012920.1(MT-ND2):m.4902A>G	rs1603219664
NC_012920.1(MT-ND2):m.4923A>T	rs1603219674
NC_012920.1(MT-ND2):m.4929C>T	rs1603219676
NC_012920.1(MT-ND2):m.4935A>C	rs1603219678
NC_012920.1(MT-ND2):m.4935A>G	rs1603219678
NC_012920.1(MT-ND2):m.4948T>C	rs1603219686
NC_012920.1(MT-ND2):m.4953A>G	rs1603219688
NC_012920.1(MT-ND2):m.4954T>C	rs1603219689
NC_012920.1(MT-ND2):m.4974G>A	rs1603219704
NC_012920.1(MT-ND2):m.5010T>C	rs1603219718
NC_012920.1(MT-ND2):m.5038T>C	rs1556422943
NC_012920.1(MT-ND2):m.5047T>C	rs1603219746
NC_012920.1(MT-ND2):m.5080A>G	rs1603219771
NC_012920.1(MT-ND2):m.5094A>G	rs1603219783
NC_012920.1(MT-ND2):m.5190A>G	rs1603219819
NC_012920.1(MT-ND2):m.5265A>G	rs1603219856
NC_012920.1(MT-ND2):m.5266T>C	rs1603219857
NC_012920.1(MT-ND2):m.5289A>G	rs1603219875
NC_012920.1(MT-ND2):m.5295C>A	rs1556422970
NC_012920.1(MT-ND2):m.5296T>C	rs1603219883
NC_012920.1(MT-ND2):m.5301A>C	rs199794187
NC_012920.1(MT-ND2):m.5310A>G	rs1603219891
NC_012920.1(MT-ND2):m.5311T>C	rs1603219892
NC_012920.1(MT-ND2):m.5320C>G	rs1603219899
NC_012920.1(MT-ND2):m.5325A>G	rs1603219901
NC_012920.1(MT-ND2):m.5444C>A	rs1603219956
NC_012920.1(MT-ND2):m.5451A>G	rs1603219965
NC_012920.1(MT-ND2):m.5496A>G	rs879099820
NC_012920.1:m.5505A>G	rs1569484003

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