List of variants reported as pathogenic for LCA5-related retinopathy by OMIM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001122769.3(LCA5):c.835C>T (p.Gln279Ter)	rs121918165	0.00006
NM_001122769.3(LCA5):c.1151del (p.Pro384fs)	rs386834252
NM_001122769.3(LCA5):c.1476dup (p.Pro493fs)	rs386834253
NM_181714.4(LCA5):c.0_-298+211del

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