The NM_000350.3(ABCA4):c.6289C>T variant in ABCA4 is a missense variant predicted to cause substitution of proline by serine at amino acid 2097 (p.Pro2097Ser). The total minor allele frequency in gnomAD v4.1.0 is 0.000001239 (2/1613554 alleles), which is lower than the ClinGen ABCA4 VCEP’s threshold for PM2_Supporting (<0.0001). The computational predictor REVEL gives a score of 0.926 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 infinity and the CI is 14.02-infinity, which is above the ABCA4 VCEP threshold of >5, where the CI does not contain 1 (PS4; PMID: 35120629). At least one patient with this variant displayed age of onset under 18 years of age, macular flecks, two ABCA4 variants found on WES, and decreased central visual acuity, which is highly specific for ABCA4-related retinopathy (PP4; PMID: 31674661). This variant has been detected in at least 2 individuals with ABCA4-related retinopathy. Of those individuals, 2 were compound heterozygous for the variant and a pathogenic variant, c.4720G>T p.(Glu1574*) and c.4605_4606insT (p.Lys1536Ter), which was not confirmed in trans (PM3; PMIDs: 31674661, 25474345). 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, PM3, PP4, PM2_Supporting, PP3_Moderate.