ClinVar Miner

List of variants in gene MT-ND4L studied for Leigh syndrome

Included ClinVar conditions (11):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-ND4L):m.10489A>G rs1603222854
NC_012920.1(MT-ND4L):m.10492T>C rs1603222857
NC_012920.1(MT-ND4L):m.10506A>G rs199688733
NC_012920.1(MT-ND4L):m.10507C>T rs1603222868
NC_012920.1(MT-ND4L):m.10522G>A rs1603222873
NC_012920.1(MT-ND4L):m.10524A>G rs1603222875
NC_012920.1(MT-ND4L):m.10530G>A rs1603222880
NC_012920.1(MT-ND4L):m.10579T>C rs1603222900
NC_012920.1(MT-ND4L):m.10599G>A rs1603222910
NC_012920.1(MT-ND4L):m.10600C>T rs1603222912
NC_012920.1(MT-ND4L):m.10602A>G rs1603222913
NC_012920.1(MT-ND4L):m.10609T>C rs200487531
NC_012920.1(MT-ND4L):m.10620A>G rs1603222915
NC_012920.1(MT-ND4L):m.10630T>C rs1603222919
NC_012920.1(MT-ND4L):m.10635G>A rs1603222924
NC_012920.1(MT-ND4L):m.10639A>G rs1603222927
NC_012920.1(MT-ND4L):m.10644G>A rs1569484385
NC_012920.1(MT-ND4L):m.10653G>A rs386829108
NC_012920.1(MT-ND4L):m.10654C>T rs1603222934
NC_012920.1(MT-ND4L):m.10677G>A rs1603222944
NC_012920.1(MT-ND4L):m.10680G>A rs1603222945
NC_012920.1(MT-ND4L):m.10686G>A rs1603222946
NC_012920.1(MT-ND4L):m.10704G>A rs28437034
NC_012920.1(MT-ND4L):m.10749A>G rs1603222963
NC_012920.1(MT-ND4L):m.10750A>G rs372297272

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