Heterozygous individuals in ABCA4 disease and control cohort harboring rare variants in macular dystrophy genes <i>CDHR1</i>, <i>CHM</i>, <i>CRX</i>, <i>ELOVL4</i>, <i>PROM1</i>, <i>PRPH2</i>, <i>ROM1</i>.

All comparisons were performed with the two-sided Fisher’s Exact Test (FET). MAF, minor allele frequency; gnomAD, genome aggregation database; CADD, combined annotation dependent depletion; nd, not detected.