List of variants reported as uncertain significance for hereditary optic atrophy by Institute of Human Genetics, University of Goettingen

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001098.3(ACO2):c.1442A>C (p.Asp481Ala)
NM_001098.3(ACO2):c.2015A>C (p.Glu672Ala)
NM_006796.3(AFG3L2):c.965A>G (p.Glu322Gly)
NM_032273.4(TMEM126A):c.329G>A (p.Gly110Asp)	rs374124838

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