List of variants reported as uncertain significance for Cone dystrophy with supernormal rod response by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_133497.4(KCNV2):c.16G>C (p.Glu6Gln)	rs143189186	0.00038
NM_133497.4(KCNV2):c.1043T>C (p.Leu348Pro)	rs201425989	0.00016
NM_133497.4(KCNV2):c.1196C>T (p.Ala399Val)	rs200444639	0.00016
NM_133497.4(KCNV2):c.38A>G (p.Tyr13Cys)	rs774058342	0.00004
NM_133497.4(KCNV2):c.326A>G (p.Gln109Arg)

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