List of variants reported as likely benign for color vision disorder by Genome-Nilou Lab

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001377295.2(GNAT2):c.370G>A (p.Val124Met)	rs41280330	0.00428
NM_019098.5(CNGB3):c.1208G>A (p.Arg403Gln)	rs147876778	0.00119
NM_001377295.2(GNAT2):c.147C>T (p.Ile49=)	rs146945932	0.00115
NM_019098.5(CNGB3):c.*125G>C	rs186370374	0.00087

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