NM_025114.4(CEP290):c.4661_4663del (p.Glu1554del) is an in-frame deletion causing a change in the length of the protein by 1 amino acid in a non-repeat region, with at least one of the deleted base pairs highly conserved with a PhyloP conservation score of 7.37 (PM4_Supporting). This variant is present in gnomAD v.4.1.1 at a total allele frequency of 0.00002232, with 36 alleles / 1,612,700 total alleles, which is lower than the ClinGen LCA/eoRD VCEP PM2_Supporting threshold of <0.0006 (PM2_Supporting). This variant has been reported in at least 1 proband with early-onset severe retinal dystrophy who was homozygous for the variant (0.5 points, PMID: 29398085). This variant has also been reported in at least 5 probands with early-onset severe retinal dystrophy who were compound heterozygous with the NM_025114.4(CEP290):c.4024C>T (p.Gln1342Ter) variant or the NM_025114.4(CEP290):c.5850del (p.Phe1950fs) variant suspected in trans (1 point, PMID: 33970760, PMID: 17345604) or with the NM_025114.4(CEP290):c.297+1G>T variant, the NM_025114.4(CEP290):c.3904C>T (p.Gln1302Ter) variant, or the NM_025114.4(CEP290):c.1219_1220del (p.Met407GlufsTer14) variant confirmed in trans (3 points, PMID: 28973549, PMID: 32165824, PMID: 34196655), which were previously classified pathogenic by the ClinGen LCA/eoRD VCEP (4.5 total points, PM3_VeryStrong). At least one proband harboring this variant exhibits a phenotype including diagnosis of Leber congenital amaurosis (0.5 pts), onset before age 5 years (0.5 pts), extinguished electroretinogram responses from rods (0.5 pts) and cones (0.5 pts), central visual acuity limited to light perception (0.5 pts), white mottling in the peripheral pigmentation (0.5 pts), absence of vasculopathy / normal optic disc color, and decreased flash visual evoked potentials, with genotyping by next-generation sequencing identifying no alternative basis for retinal disease (2 pts), which together are specific for CEP290-related ciliopathy (total 5 points, PMID: 33970760, PP4). The variant has been reported to segregate with childhood-onset severe retinal dystrophy through the proband plus 2 similarly affected relatives, with the variant present in the homozygous state (PP1_Moderate; PMID: 29398085). In summary, this variant meets the criteria to be classified as Pathogenic for CEP290-related ciliopathy based on the ACMG/AMP criteria applied, as specified by the ClinGen LCA/eoRD VCEP: PM4_Supporting, PM2_Supporting, PM3_Very-Strong, PP1_Moderate, and PP4. (LCA/eoRD VCEP Specifications for CEP290 Version 1.0.0)