List of variants reported as benign for color vision disorder by Molecular Genetics Laboratory, Institute for Ophthalmic Research

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.72T>C (p.Asp24=)	rs6727412	0.13838
NM_001298.3(CNGA3):c.592G>A (p.Glu198Lys)	rs2271041	0.01129
NM_001298.3(CNGA3):c.353A>G (p.Gln118Arg)	rs142837782	0.00305
NM_001298.3(CNGA3):c.102-16A>G	rs2279859
NM_001298.3(CNGA3):c.215+151T>C	rs937725

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