ClinVar Miner

List of variants in gene MT-ND1 reported as uncertain significance for Leigh syndrome

Included ClinVar conditions (11):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-ND1):m.3307A>T rs1603218882
NC_012920.1(MT-ND1):m.3308delinsAC rs1603218887
NC_012920.1(MT-ND1):m.3310C>T rs1603218889
NC_012920.1(MT-ND1):m.3313A>G rs1603218891
NC_012920.1(MT-ND1):m.3316G>C rs2853516
NC_012920.1(MT-ND1):m.3320A>G rs1603218896
NC_012920.1(MT-ND1):m.3328C>T rs1603218901
NC_012920.1(MT-ND1):m.3357G>C rs1556422714
NC_012920.1(MT-ND1):m.3358G>A rs1556422715
NC_012920.1(MT-ND1):m.3395A>C rs1556422722
NC_012920.1(MT-ND1):m.3419A>G rs1603218949
NC_012920.1(MT-ND1):m.3427G>A rs1603218960
NC_012920.1(MT-ND1):m.3488T>C rs1603218982
NC_012920.1(MT-ND1):m.3496G>A rs1603218984
NC_012920.1(MT-ND1):m.3508A>G rs1603218990
NC_012920.1(MT-ND1):m.3509T>C rs1603218992
NC_012920.1(MT-ND1):m.3526G>A rs1603218998
NC_012920.1(MT-ND1):m.3569C>T rs1603219022
NC_012920.1(MT-ND1):m.3607G>A rs1556422761
NC_012920.1(MT-ND1):m.3622C>A rs1603219048
NC_012920.1(MT-ND1):m.3643G>A rs1603219061
NC_012920.1(MT-ND1):m.3652A>G rs1603219066
NC_012920.1(MT-ND1):m.3653T>C rs1603219067
NC_012920.1(MT-ND1):m.3661T>G rs1603219070
NC_012920.1(MT-ND1):m.3670G>A rs1603219074
NC_012920.1(MT-ND1):m.3701C>T rs1603219086
NC_012920.1(MT-ND1):m.3709G>A rs1603219090
NC_012920.1(MT-ND1):m.3710C>T rs1603219093
NC_012920.1(MT-ND1):m.3712G>A rs1603219095
NC_012920.1(MT-ND1):m.3713T>C rs1603219096
NC_012920.1(MT-ND1):m.3715G>A rs1603219097
NC_012920.1(MT-ND1):m.3749T>C rs1603219116
NC_012920.1(MT-ND1):m.3751A>G rs1603219119
NC_012920.1(MT-ND1):m.3764C>T rs1603219127
NC_012920.1(MT-ND1):m.3772A>G rs1603219135
NC_012920.1(MT-ND1):m.3775A>T rs1603219137
NC_012920.1(MT-ND1):m.3793T>C rs1603219148
NC_012920.1(MT-ND1):m.3887A>G rs1603219185
NC_012920.1(MT-ND1):m.3910G>A rs1603219195
NC_012920.1(MT-ND1):m.3937T>C rs1603219204
NC_012920.1(MT-ND1):m.4055T>C rs1603219279
NC_012920.1(MT-ND1):m.4082T>C rs1603219291
NC_012920.1(MT-ND1):m.4094C>T rs1603219299
NC_012920.1(MT-ND1):m.4105A>G rs1603219306
NC_012920.1(MT-ND1):m.4148G>A rs1603219323
NC_012920.1(MT-ND1):m.4153G>A rs28566134
NC_012920.1(MT-ND1):m.4165C>G rs1603219331
NC_012920.1(MT-ND1):m.4180A>G rs1603219342
NC_012920.1(MT-ND1):m.4193T>C rs1603219346
NC_012920.1(MT-ND1):m.4211T>C rs1603219356
NC_012920.1(MT-ND1):m.4238T>C rs1603219369
NC_012920.1(MT-ND1):m.4247T>C rs1603219376
NC_012920.1(MT-ND1):m.4258A>G rs1603219383
NC_012920.1:m.3928G>C rs587776442

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