List of variants reported as likely pathogenic for color vision disorder by DBGen Ocular Genomics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.1168_1169del (p.Leu390fs)
NM_001298.3(CNGA3):c.1451A>C (p.Gln484Pro)
NM_001298.3(CNGA3):c.580G>T (p.Glu194Ter)
NM_006204.4(PDE6C):c.2254G>A (p.Glu752Lys)	rs2133878975
NM_025136.4(OPA3):c.206A>C (p.Lys69Thr)	rs760083523

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