List of variants reported as pathogenic for optic atrophy by Institute of Human Genetics, University Hospital of Duesseldorf

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_032317.3(DNAJC30):c.152A>G (p.Tyr51Cys)	rs61732167	0.00112
NM_152296.5(ATP1A3):c.2266C>T (p.Arg756Cys)	rs1064797245

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