List of variants reported as pathogenic for color vision disorder by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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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.1279C>T (p.Arg427Cys)	rs141386891	0.00036
NM_001298.3(CNGA3):c.1306C>T (p.Arg436Trp)	rs104893621	0.00003
NC_000001.11:g.161781912dup	rs1553227755

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