List of variants reported as uncertain significance for hereditary optic atrophy by Juno Genomics, Hangzhou Juno Genomics, Inc

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_025136.4(OPA3):c.11G>A (p.Gly4Asp)
NM_025136.4(OPA3):c.308G>A (p.Arg103His)
NM_152296.5(ATP1A3):c.2146AAG[1] (p.Lys717del)	rs1064795403

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