List of variants reported as uncertain significance for cone-rod dystrophy by Ophthalmic Genetics Group, Institute of Molecular and Clinical Ophthalmology Basel

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000350.3(ABCA4):c.4340A>T (p.Glu1447Val)	rs2101034896
NM_001371596.2(MFSD8):c.1445G>C (p.Arg482Pro)
NM_201253.3(CRB1):c.1838_1840dup (p.Leu613_Gly614insVal)	rs2125471114
NM_201253.3(CRB1):c.2980A>G (p.Lys994Glu)	rs2125499116

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