List of variants in gene MT-ND1 reported as pathogenic for Leber optic atrophy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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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.3635G>A	rs397515507
NC_012920.1(MT-ND1):m.3697G>A	rs199476122
NC_012920.1(MT-ND1):m.3733G>A	rs199476125
NC_012920.1(MT-ND1):m.4136A>G	rs199476121
NC_012920.1(MT-ND1):m.4160T>C	rs199476119
NC_012920.1(MT-ND1):m.4171C>A	rs28616230
NC_012920.1(MT-ND1):m.4216T>C	rs1599988

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