Figure 5 of Sun, Mol Vis 2020; 26:588-602.

Figure 5. Frequencies of variants in the six genes in Caucasian and Asian patients. A: Potential pathogenic variants (PPVs) in CNGA3 were the most common among Asians and involved the common achromatopsia (ACHM) and cone-rod dystrophy (CORD), as well as the rare Leber congenital amaurosis (LCA), unclassified retinopathy (UN), and retinitis pigmentosa (RP). B: Among Caucasians, PPVs in CNGB3 were the most common, and these variants are associated with ACHM, which is the most common disease, as well as with CORD, UN, LCA, oligocone trichromacy (OT), and macular dystrophy (MD).