List of variants reported as pathogenic for Autosomal dominant optic atrophy classic form by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_130837.3(OPA1):c.1734dup (p.Gln579fs)	rs1560377736
NM_130837.3(OPA1):c.1935+1G>C	rs1711518217
NM_130837.3(OPA1):c.2051C>G (p.Ser684Ter)	rs2109138909
NM_130837.3(OPA1):c.2873_2876del	rs80356530
NM_130837.3(OPA1):c.902T>G (p.Leu301Ter)	rs1488795500

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