List of variants in gene CEP290 reported as likely benign for Leber congenital amaurosis 10

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_025114.4(CEP290):c.4119A>G (p.Lys1373=)	rs117122459	0.02377
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.1624-5T>C	rs142742071	0.00704
NM_025114.4(CEP290):c.5199A>G (p.Gln1733=)	rs79644671	0.00692
NM_025114.4(CEP290):c.6401T>C (p.Ile2134Thr)	rs117852025	0.00488

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