List of variants in gene CEP290 reported as likely benign by Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille

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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_025114.4(CEP290):c.5185C>T (p.Arg1729Trp)	rs201353893	0.00031
NM_025114.4(CEP290):c.2615C>T (p.Ser872Leu)	rs373341530	0.00030
NM_025114.4(CEP290):c.1038T>G (p.Asp346Glu)	rs372923864	0.00001
NM_025114.4(CEP290):c.2320G>C (p.Ala774Pro)	rs777365811	0.00001
NM_025114.4(CEP290):c.6818+5G>A	rs935214183	0.00001
NM_025114.4(CEP290):c.181-3T>C	rs770415774
NM_025114.4(CEP290):c.4777G>A (p.Asp1593Asn)	rs1201073418

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