List of variants reported as pathogenic for color vision disorder by Illumina Laboratory Services, Illumina

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.848G>A (p.Arg283Gln)	rs104893614	0.00010
NM_001298.3(CNGA3):c.1228C>T (p.Arg410Trp)	rs137852608	0.00004
NM_001298.3(CNGA3):c.1585G>A (p.Val529Met)	rs104893619	0.00004
NM_001298.3(CNGA3):c.67C>T (p.Arg23Ter)	rs777509481	0.00003

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