List of variants in gene CEP290 reported as benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_025114.4(CEP290):c.2268A>G (p.Ser756=)	rs2468255	0.91372
NM_025114.4(CEP290):c.853-12_853-11insG	rs71082425	0.87640
NM_025114.4(CEP290):c.5237G>A (p.Arg1746Gln)	rs61941020	0.00714
NM_025114.4(CEP290):c.6522+5dup	rs11405846

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