ClinVar Miner

List of variants in gene MT-ND3 studied for Leigh syndrome

Included ClinVar conditions (11):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-ND3):m.10083A>G rs1556423760
NC_012920.1(MT-ND3):m.10084T>C rs41487950
NC_012920.1(MT-ND3):m.10086A>G rs28358274
NC_012920.1(MT-ND3):m.10098G>T rs1569484342
NC_012920.1(MT-ND3):m.10110A>G rs1603222674
NC_012920.1(MT-ND3):m.10111T>C rs1603222676
NC_012920.1(MT-ND3):m.10113A>G rs1603222679
NC_012920.1(MT-ND3):m.10143G>A rs202131419
NC_012920.1(MT-ND3):m.10146T>C rs1603222696
NC_012920.1(MT-ND3):m.10158T>A rs199476117
NC_012920.1(MT-ND3):m.10159C>A rs1603222701
NC_012920.1(MT-ND3):m.10188A>G rs1603222715
NC_012920.1(MT-ND3):m.10192C>A rs1556423776
NC_012920.1(MT-ND3):m.10192C>T rs1556423776
NC_012920.1(MT-ND3):m.10203G>A rs1556423781
NC_012920.1(MT-ND3):m.10225T>C rs1603222726
NC_012920.1(MT-ND3):m.10236A>G rs1603222731
NC_012920.1(MT-ND3):m.10266G>A rs1603222746
NC_012920.1(MT-ND3):m.10269C>A rs1603222748
NC_012920.1(MT-ND3):m.10320G>A rs28358276
NC_012920.1(MT-ND3):m.10321T>C rs193302928
NC_012920.1(MT-ND3):m.10324T>C rs1603222776
NC_012920.1(MT-ND3):m.10326T>A rs1603222777
NC_012920.1(MT-ND3):m.10326T>C rs1603222777
NC_012920.1(MT-ND3):m.10329T>C rs878943163
NC_012920.1(MT-ND3):m.10345T>C rs201397417
NC_012920.1(MT-ND3):m.10348T>C rs1556423803
NC_012920.1(MT-ND3):m.10353G>A rs28435660
NC_012920.1(MT-ND3):m.10365G>A rs1603222800
NC_012920.1(MT-ND3):m.10366C>T rs1603222801
NC_012920.1(MT-ND3):m.10371G>A rs1603222803
NC_012920.1(MT-ND3):m.10398A>T rs2853826
NC_012920.1(MT-ND3):m.10399C>T rs1603222820
NC_012920.1(MT-ND3):m.10401G>A rs28719882
NC_012920.1:m.10134C>A rs587780529
NC_012920.1:m.10254G>A rs587776438
m.10158T>C rs199476117
m.10191T>C rs267606890
m.10197G>A rs267606891
m.10237T>C rs1556423787
m.10398A>G rs2853826

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