The list of genes implicated in hair greying phenotype include loci previously linked with smoking status (KIF1A, RUNX1, IRF4, BRINP1, TEX41, GRID1), BMI/obesity (GRID1, TEX41, SEMA4D, TBC1D22A, RUNX1), bone mineral density (RUNX1, TBC1D22A, TEX41), cardiovascular diseases (FGF5, MROH2A, DPEP1, GRID1) and immunology (RUNX1, TBC1D22A, IRF4, TMEM132C, GRID1). Importantly, all the above mentioned factors (particularly smoking) were linked with hair greying syndrome in previous research and therefore the link between these genes and greying seems to be justified [16, 33–36]. The gene discussed is TBC1D22A; the disease is obesity due to melanocortin 4 receptor deficiency.