List of variants reported as likely pathogenic for optic atrophy by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_004204.5(PIGQ):c.619C>T (p.Arg207Ter)	rs730882240	0.00002
NM_130837.3(OPA1):c.1262G>A (p.Arg421Gln)	rs535885178	0.00001
NM_194279.4(ISCA2):c.229G>A (p.Gly77Ser)	rs730882246

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