List of variants reported as likely benign for Leber congenital amaurosis 5

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001122769.3(LCA5):c.*1528G>A	rs41269343	0.11829
NM_001122769.3(LCA5):c.*1300G>A	rs16890805	0.02447
NM_001122769.3(LCA5):c.*1495G>A	rs76104104	0.02321
NM_001122769.3(LCA5):c.1642C>T (p.Pro548Ser)	rs185347145	0.00042
NM_001122769.3(LCA5):c.768G>A (p.Gln256=)	rs142495741	0.00024
NM_001122769.3(LCA5):c.1099-12A>G	rs192066914	0.00016
NM_001122769.3(LCA5):c.1260G>A (p.Lys420=)	rs141642284	0.00012
NM_001122769.3(LCA5):c.1800A>G (p.Lys600=)	rs147032284	0.00004
NM_001122769.3(LCA5):c.1518C>T (p.Pro506=)	rs769091728	0.00001
NM_001122769.3(LCA5):c.1242A>G (p.Arg414=)	rs1769717155
NM_001122769.3(LCA5):c.1769A>G (p.Asp590Gly)	rs771460783
NM_001122769.3(LCA5):c.1785T>A (p.Ile595=)	rs544388502
NM_001122769.3(LCA5):c.642C>T (p.His214=)	rs541395332
NM_001122769.3(LCA5):c.735C>T (p.Asn245=)	rs781334192
NM_001122769.3(LCA5):c.759C>T (p.Phe253=)	rs528612334
NM_001122769.3(LCA5):c.859-12G>C	rs115317386

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