Further, SLCO1B1 variations c.388G > A (p.N130D, rs2306283) and c.521T > C (p.V174A, rs4149056) were also found to be risk factors for neonatal unconjugated hyperbilirubinemia (Huang et al., 2004; D'Silva et al., 2014). The gene discussed is SLCO1B1; the disease is Hyperbilirubinemia.