ClinVar Miner

List of variants studied for hereditary optic atrophy by Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-ND1):m.3460G>A rs199476118
NC_012920.1(MT-ND4):m.11777C>A rs28384199
NC_012920.1(MT-ND4):m.11778G>A rs199476112
NC_012920.1(MT-ND5):m.13042G>A rs267606898
NC_012920.1(MT-ND5):m.13051G>A rs1131692063
NC_012920.1(MT-ND6):m.14484T>C rs199476104
m.10663T>C rs1556423844
m.3635G>A rs397515507
m.4171C>A rs28616230

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