However, it was to be the highest (29.31 ng/mL) in relation to others in two representatives of the rarest genotype TT-CC/DBP isotype Gc1F/1F variant, and the lowest (21.53 ng/mL)—in representatives of references genotype TG-CA, coding DBP isotype Gc1S/2 and constituting 45% of the experimental MS cohort. The gene discussed is DBP; the disease is myeloid sarcoma.