List of variants reported as uncertain significance for color vision disorder by Fulgent Genetics, Fulgent Genetics

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_019098.5(CNGB3):c.1492T>A (p.Leu498Met)	rs115246141	0.00350
NM_001298.3(CNGA3):c.1034A>G (p.His345Arg)	rs780411290	0.00011
NM_019098.5(CNGB3):c.2047A>C (p.Thr683Pro)	rs144474033	0.00009
NM_019098.5(CNGB3):c.2245A>G (p.Lys749Glu)	rs190864281	0.00008
NM_019098.5(CNGB3):c.1696C>T (p.His566Tyr)	rs144605411	0.00004
NM_006204.4(PDE6C):c.101G>A (p.Gly34Glu)	rs772889663	0.00003
NM_019098.5(CNGB3):c.2103G>C (p.Gln701His)	rs770214046	0.00003
NM_001298.3(CNGA3):c.1615G>A (p.Val539Met)	rs374275399	0.00002
NM_006204.4(PDE6C):c.304C>T (p.Arg102Trp)	rs375795507

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