List of variants in gene CEP290 reported as benign by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_025114.4(CEP290):c.2055T>C (p.Ala685=)	rs45465996	0.11965
NM_025114.4(CEP290):c.3710G>A (p.Arg1237His)	rs7307793	0.05381
NM_025114.4(CEP290):c.442-19T>A	rs113132803	0.05334
NM_025114.4(CEP290):c.2512A>G (p.Lys838Glu)	rs11104738	0.05247
NM_025114.4(CEP290):c.4119A>G (p.Lys1373=)	rs117122459	0.02390
NM_025114.4(CEP290):c.1991A>G (p.Asp664Gly)	rs79705698	0.02050
NM_025114.4(CEP290):c.829G>C (p.Glu277Gln)	rs45502896	0.01608
NM_025114.4(CEP290):c.5237G>A (p.Arg1746Gln)	rs61941020	0.00577
NM_025114.4(CEP290):c.5322C>T (p.Leu1774=)	rs117370446	0.00329
NM_025114.4(CEP290):c.6522+5dup	rs11405846

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