The NM_000350.3:c.1957C>T variant in ABCA4 is a missense variant predicted to cause substitution of arginine by cysteine at amino acid 653 (p.Arg653Cys). The total minor allele frequency in gnomAD v4.1.0 is 0.00002666 (43/1612644 alleles), which is lower than the ClinGen ABCA4 VCEP’s threshold for PM2_Supporting (<0.0001). The computational predictor REVEL gives a score of 0.852 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. The OR is 139.4 and the CI is 43.93-707.41, 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 at least 4 individuals with ABCA4-related retinopathy. Of those individuals, 2 were compound heterozygous for the variant and a pathogenic or likely pathogenic variant unconfirmed in trans (c.3386G>T; p.(Arg1129Leu)( PM3; PMID:35119454). ATPase activity in HEK293 cells showed reduction by over 20% 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 1.0.0): PS4, PP3_Moderate, PM3, PM2_Supporting, PS3_Supporting.