Figure 2. Variants in the solute carrier family 4, sodium borate transporter, member 11 (SLC4A11) gene on chromosome 20p13 that have been detected in patients with Fuchs endothelial corneal dystrophy (FECD). The gene is drawn from 3′ to 5′ reflecting its physical orientation on the reverse strand of the reference genome. Figure drawn as described in the caption for Figure 1, with the red font indicating variants identified in our African American FECD cases and variants marked with an asterisk (*) indicating newly identified variants in African Americans with FECD that have not been previously reported in patients with FECD.