List of variants reported as uncertain significance for optic atrophy by New York Genome Center

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_032730.5(RTN4IP1):c.254C>T (p.Pro85Leu)	rs193121821	0.00016
NM_152296.5(ATP1A3):c.1906G>A (p.Ala636Thr)	rs782744167	0.00001

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