List of variants in gene CRB1 reported as benign for Leber congenital amaurosis

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_201253.3(CRB1):c.1410A>G (p.Leu470=)	rs3902057	0.92528
NM_201253.3(CRB1):c.2677-8C>T	rs73071678	0.00970
NM_201253.3(CRB1):c.1470C>T (p.Gly490=)	rs35193230	0.00265
NM_201253.3(CRB1):c.2306G>A (p.Arg769His)	rs62636287	0.00208
NM_201253.3(CRB1):c.2103C>G (p.Pro701=)	rs144436610	0.00104
NM_201253.3(CRB1):c.1533C>T (p.Ala511=)	rs142224492	0.00051
NM_201253.3(CRB1):c.1075T>G (p.Ser359Ala)	rs533227950	0.00007
NM_201253.3(CRB1):c.3258T>A (p.Ala1086=)	rs535494663

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