List of variants reported as likely pathogenic for color vision disorder by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001298.3(CNGA3):c.485A>T (p.Asp162Val)	rs747447519	0.00010
NM_001298.3(CNGA3):c.1085C>T (p.Thr362Ile)	rs1574390811
NM_007348.4(ATF6):c.1720-2A>T
NM_007348.4(ATF6):c.1805-2A>C
NM_019098.5(CNGB3):c.806T>C (p.Leu269Pro)	rs1189928623

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