List of variants reported as uncertain significance for Infantile cerebellar-retinal degeneration; Optic atrophy 9

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001098.3(ACO2):c.220C>G (p.Leu74Val)	rs141772938	0.00383
NM_001098.3(ACO2):c.719G>C (p.Gly240Ala)	rs141878785	0.00064
NM_001098.3(ACO2):c.2051G>A (p.Arg684Gln)	rs200345386	0.00011
NM_001098.3(ACO2):c.2050C>T (p.Arg684Trp)	rs768950391	0.00006
NM_001098.3(ACO2):c.36+262C>T

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