List of variants in gene MT-CYB reported as uncertain significance for 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: 3

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.14795T>C	rs1603224896
NC_012920.1(MT-CYB):m.15257G>A	rs41518645
NC_012920.1(MT-CYB):m.15437G>A	rs878853058

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