List of variants in gene CEP290 reported as benign by Eurofins Ntd Llc (ga)

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: 14

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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.2055T>C (p.Ala685=)	rs45465996	0.11965
NM_025114.4(CEP290):c.442-19T>A	rs113132803	0.05166
NM_025114.4(CEP290):c.5709+18C>A	rs7973969	0.05003
NM_025114.4(CEP290):c.251-10A>T	rs190383141	0.02052
NM_025114.4(CEP290):c.829G>C (p.Glu277Gln)	rs45502896	0.01608
NM_025114.4(CEP290):c.5237G>A (p.Arg1746Gln)	rs61941020	0.00714
NM_025114.4(CEP290):c.5506A>G (p.Ile1836Val)	rs11104729	0.00463
NM_025114.4(CEP290):c.1522+6C>T	rs148446546	0.00371
NM_025114.4(CEP290):c.5322C>T (p.Leu1774=)	rs117370446	0.00329
NM_025114.4(CEP290):c.6960+10G>A	rs75011402	0.00305
NM_025114.4(CEP290):c.6452T>C (p.Leu2151Ser)	rs191613017	0.00032
NM_025114.4(CEP290):c.3574-9del	rs10717563
NM_025114.4(CEP290):c.6522+5dup	rs11405846

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