ClinVar Miner

List of variants in gene MT-ND1 studied for hereditary optic atrophy

Included ClinVar conditions (34):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NC_012920.1(MT-ND1):m.3394T>C rs41460449
NC_012920.1(MT-ND1):m.3460G>A rs199476118
NC_012920.1(MT-ND1):m.3697G>A rs199476122
NC_012920.1(MT-ND1):m.4025C>T rs397515509
NC_012920.1(MT-ND1):m.4136A>G rs199476121
NC_012920.1(MT-ND1):m.4160T>C rs199476119
NC_012920.1(MT-ND1):m.4216T>C rs1599988
m.3376G>A rs397515612
m.3635G>A rs397515507
m.3700G>A rs397515508
m.3733G>A rs199476125
m.4171C>A rs28616230

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