ClinVar Miner

List of variants in gene MT-TC studied for hereditary skeletal muscle disorder

Included ClinVar conditions (587):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-TC):m.5772G>A rs1556423031
NC_012920.1(MT-TC):m.5773G>A rs9659239
NC_012920.1(MT-TC):m.5774T>C rs1603220102
NC_012920.1(MT-TC):m.5774T>G rs1603220102
NC_012920.1(MT-TC):m.5775T>C rs1603220105
NC_012920.1(MT-TC):m.5780G>A rs878999194
NC_012920.1(MT-TC):m.5783G>A rs1603220110
NC_012920.1(MT-TC):m.5785T>C rs373493739
NC_012920.1(MT-TC):m.5786T>C rs1603220117
NC_012920.1(MT-TC):m.5786dup rs1603220115
NC_012920.1(MT-TC):m.5788T>C rs1556423033
NC_012920.1(MT-TC):m.5791G>A rs1603220121
NC_012920.1(MT-TC):m.5793A>G rs1603220122
NC_012920.1(MT-TC):m.5794T>C rs1556423035
NC_012920.1(MT-TC):m.5800A>G rs1603220125
NC_012920.1(MT-TC):m.5802T>C rs1603220128
NC_012920.1(MT-TC):m.5804A>G rs1603220130
NC_012920.1(MT-TC):m.5806T>C rs879211572
NC_012920.1(MT-TC):m.5807A>G rs386828978
NC_012920.1(MT-TC):m.5809G>A rs1603220134
NC_012920.1(MT-TC):m.5811A>G rs1603220136
NC_012920.1(MT-TC):m.5814T>A rs200077222
NC_012920.1(MT-TC):m.5814T>C rs200077222
NC_012920.1(MT-TC):m.5817C>T rs1603220138
NC_012920.1(MT-TC):m.5819T>C rs1603220139
NC_012920.1(MT-TC):m.5821G>A rs56133209
NC_012920.1(MT-TC):m.5822G>A rs1556423041
NC_012920.1(MT-TC):m.5823A>G rs878875817
NC_012920.1(MT-TC):m.5824G>A rs879140945

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