List of variants in gene CEP290 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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.4805C>T (p.Thr1602Met)	rs369451049	0.00006
NM_025114.4(CEP290):c.1711G>A (p.Gly571Arg)
NM_025114.4(CEP290):c.2594T>C (p.Leu865Pro)	rs1468696400
NM_025114.4(CEP290):c.64GAA[1] (p.Glu23del)	rs780211907

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