In addition, we found an association with rs3217882, located in an intron of cyclin D2 (CCND2), which was associated with an increased risk of exclusive BCC development (OR 1.43; 95%CI 1.12–1.82, P = 0.004) and SNP rs970318 in PRKACB associated with exclusive BCC diagnosis (OR 0.72; 95% CI 0.56–0.92, P = 0.009). The gene discussed is CCND2; the disease is skin basal cell carcinoma.