Two major genes on chromosome 15 affect the quantity and quality of the melanin produced by melanogenesis. HERC2, a large ubiquitin ligase, contains the promoter region for OCA2, the P protein. When a T is replaced with a C in rs12913832 of intron 86, OCA2 transcription is depressed, resulting in a blue-eyed individual. This epistatic relationship demonstrates the significance of introns and how a single-base change greatly affects an aspect of the individual. OCA2 contains regions for the numerous eye colors, but one SNP is a strong predictor for brown/blue eyes. A change in rs1800407 causes a change in the protein, Arg419Gln, and a change from brown to blue eyes. Therefore, the residue change causes a problem with the P protein, and melanin maturation decreases. Aside from these two genes, the genes involved in melanogenesis and other minor genes also contain regions that account for eye color. Having little effect on eye color, many of them deal primarily with hair and skin pigmentation. Lastly, disorders involved in eye color include ocular albinism and heterochromia. Depending on how little pigment the melanocytes produce, albinism causes red or violet eyes. Producing multicolored irises, heterochromia stems from mutations in certain cells of the iris.
https://www.nature.com/articles/jhg2010126