The association study in the Czech population indicated ancestral susceptibility to the risk of CRC for the missense AGT SNP rs699 and to the 3’UTR SNP rs10211 in CYP3A7. Interestingly, SNPs in these two genes feature similar phenotypic effects, such as predisposing to hypertension and salt sensitivity [18]. The gene discussed is CYP3A7; the disease is hypertensive disorder.