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]. This evidence concerns the gene MROH2A and obesity due to melanocortin 4 receptor deficiency.