List of variants in gene MT-ND5 reported as pathogenic 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: 11

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ND5):m.12338T>C	rs201863060
NC_012920.1(MT-ND5):m.12425del	rs1603223730
NC_012920.1(MT-ND5):m.12706T>C (p.Phe124Leu)	rs267606893
NC_012920.1(MT-ND5):m.13042G>A	rs267606898
NC_012920.1(MT-ND5):m.13045A>C	rs267606895
NC_012920.1(MT-ND5):m.13051G>A	rs1131692063
NC_012920.1(MT-ND5):m.13063G>A	rs1603224017
NC_012920.1(MT-ND5):m.13094T>C	rs1603224029
NC_012920.1(MT-ND5):m.13708G>A	rs28359178
NC_012920.1(MT-ND5):m.13730G>A	rs387906425
m.12848C>T	rs267606899

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