List of variants in gene CEP290 reported as benign for Meckel-Gruber syndrome

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_025114.4(CEP290):c.853-12_853-11insG	rs71082425	0.87640
NM_025114.4(CEP290):c.3574-9del	rs10717563
NM_025114.4(CEP290):c.6522+5dup	rs11405846

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