Another Novel SNP rs6976701 of LEP 5′-UTR was observed with its heterozygous genotype (AG) in five subjects with obesity (P055, P203, P286, P288, and P289) and homozygous recessive genotype (AA) in one subject with obesity (P292) (Figures 2(a)–2(h)). The gene discussed is LEP; the disease is obesity due to melanocortin 4 receptor deficiency.