List of variants reported as likely pathogenic for optic atrophy by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 3q29(chr3:193343827-194599635)x1
NM_130837.3(OPA1):c.2051C>G (p.Ser684Ter)	rs2109138909
NM_130837.3(OPA1):c.2778+1G>A

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