List of variants reported as likely pathogenic for optic atrophy by Institute of Medical Molecular Genetics, University of Zurich

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_130837.3(OPA1):c.1890_1891del (p.Glu630fs)	rs1711513680
NM_130837.3(OPA1):c.2873_2876del	rs80356530
NM_130837.3(OPA1):c.2987A>C (p.Lys996Thr)	rs1721758840

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