List of variants in gene CEP290 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_025114.4(CEP290):c.5237G>A (p.Arg1746Gln)	rs61941020	0.00714
NM_025114.4(CEP290):c.6401T>C (p.Ile2134Thr)	rs117852025	0.00488
NM_025114.4(CEP290):c.5506A>G (p.Ile1836Val)	rs11104729	0.00463
NM_025114.4(CEP290):c.4237G>C (p.Asp1413His)	rs183655276	0.00187
NM_025114.4(CEP290):c.1825-17CT[2]	rs367600498
NM_025114.4(CEP290):c.2484-18GTTTT[4]	rs745522483

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