List of variants reported as uncertain significance for Optic atrophy 10 with or without ataxia, intellectual disability, and seizures

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_032730.5(RTN4IP1):c.254C>T (p.Pro85Leu)	rs193121821	0.00016
NM_032730.5(RTN4IP1):c.92G>C (p.Arg31Thr)	rs1327054264	0.00001
NM_032730.5(RTN4IP1):c.-328G>T
NM_032730.5(RTN4IP1):c.104_117delinsGAAGGATT (p.Thr35_Arg39delinsArgArgIle)	rs2114690778
NM_032730.5(RTN4IP1):c.275-1299T>C
NM_032730.5(RTN4IP1):c.475G>T (p.Val159Phe)
NM_032730.5(RTN4IP1):c.508C>T (p.Pro170Ser)	rs2114677058
NM_032730.5(RTN4IP1):c.743G>T (p.Gly248Val)

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