However, sequencing of UGT1A1 has been undertaken in SCD cohorts in Guadeloupe, Portugal, Jamaica, India and the United States; genotyping of 324 SCD children from the Cooperative Study of Sickle Cell Disease (CSSCD) revealed that the common (TA)6 and (TA)7 alleles were present in 75% [10]–[15]. This evidence concerns the gene UGT1A1 and Schnyder corneal dystrophy.