List of variants reported as likely pathogenic for color vision disorder by Revvity Omics, Revvity

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.101+1G>A	rs147118493	0.00014
NM_001298.3(CNGA3):c.1688G>A (p.Arg563His)	rs552069173	0.00004
NM_019098.5(CNGB3):c.1131T>G (p.Tyr377Ter)
NM_019098.5(CNGB3):c.2085del (p.Lys695fs)	rs1585942791

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