List of variants reported as pathogenic for color vision disorder by Institute of Human Genetics, University of Leipzig Medical Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_019098.5(CNGB3):c.1148del (p.Thr383fs)	rs397515360	0.00183
NM_001298.3(CNGA3):c.1088T>C (p.Leu363Pro)
NM_001298.3(CNGA3):c.1708A>G (p.Ser570Gly)	rs2104249895
NM_006204.4(PDE6C):c.1669C>T (p.Arg557Ter)	rs781699886

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