List of variants in gene MT-ND6 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: 5

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND6):m.14482C>A	rs199476108
NC_012920.1(MT-ND6):m.14484T>C	rs199476104
NC_012920.1(MT-ND6):m.14487T>C	rs199476109
m.14495A>G	rs199476106
m.14568C>T	rs397515506

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