The NM_000350.3(ABCA4):c.2453G>A variant in ABCA4 is a missense variant predicted to cause substitution of glycine by glutamic acid at amino acid 818 (p.Gly818Glu). The total minor allele frequency in gnomAD v4.1.0 is 0.00004151 (67/1614030 alleles), which is lower than the ClinGen ABCA4 VCEP’s threshold for PM2_Supporting (<0.0001). The computational predictor REVEL gives a score of 0.937 which is above the threshold of >0.772, evidence that predicts a damaging effect on ABCA4 function (PP3_Moderate). The prevalence of the variant in affected individuals is significantly increased compared with the prevalence in controls with an OR = 12.7 and the CI is 5.89-27.63, which is above the ABCA4 VCEP threshold of >5, where the CI does not contain 1 (PS4; PMID: 35120629). This variant has been detected in multiple individuals with ABCA4-related retinopathy. Of those individuals, 1 was compound heterozygous for the variant and a pathogenic variant ([A1038V;L541P]) that was not confirmed in trans (PMID: 19074458), and another individual was homozygous for the variant (PM3; PMID: 23419329). ABCA4 expression in HEK293 cells showed a reduction to 40%-52% of wild-type ABCA4 and ATPase activity was 63 ± 5% compared to wild-type indicating that this variant impacts protein function (PS3_Supporting; PMID:33375396). In summary, this variant meets the criteria to be classified as pathogenic for ABCA4-related retinopathy based on the ACMG/AMP criteria applied, as specified by the ClinGen ABCA4 VCEP (Specification Version 1.0): PS4, PM3, PP3_Moderate, PM2_Supporting, PS3_Supporting.