List of variants reported as benign for Leber congenital amaurosis 5

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001122769.3(LCA5):c.71T>C (p.Leu24Ser)	rs2655655	0.84544
NM_001122769.3(LCA5):c.-62A>G	rs2803195	0.84542
NM_001122769.3(LCA5):c.*223A>G	rs2292109	0.45638
NM_001122769.3(LCA5):c.1967G>A (p.Gly656Asp)	rs1875845	0.36167
NM_001122769.3(LCA5):c.77A>C (p.Asp26Ala)	rs34068461	0.14840
NM_001122769.3(LCA5):c.-334C>T	rs116580217	0.01110
NM_001122769.3(LCA5):c.*1292A>G	rs77354230	0.01061

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