List of variants reported as uncertain significance for GPR179-related retinopathy by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001004334.4(GPR179):c.959G>A (p.Arg320Gln)	rs189931659	0.00194
NM_001004334.4(GPR179):c.3752C>T (p.Ser1251Leu)	rs368643450	0.00034
NM_001004334.4(GPR179):c.2908C>A (p.Pro970Thr)	rs372139002	0.00001
NM_001004334.4(GPR179):c.3460C>T (p.Gln1154Ter)	rs757044884

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