List of variants in gene LCA5 reported as likely benign for Leber congenital amaurosis 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001122769.3(LCA5):c.1215T>G (p.Val405=)	rs41270545	0.00050
NM_001122769.3(LCA5):c.338A>G (p.Asn113Ser)	rs181890907	0.00020
NM_001122769.3(LCA5):c.1746C>T (p.Asn582=)	rs183011135	0.00014
NM_001122769.3(LCA5):c.222A>T (p.Pro74=)	rs148386543	0.00014
NM_001122769.3(LCA5):c.1099-9G>A	rs546754454	0.00003
NM_001122769.3(LCA5):c.1668C>T (p.Tyr556=)	rs376479835	0.00003
NM_001122769.3(LCA5):c.897T>C (p.Ser299=)	rs767145624	0.00003

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