rs2306283, SLCO1B1

N. diseases: 16
Disease: Hyperbilirubinemia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperbilirubinemia
CUI: C0020433
Disease: Hyperbilirubinemia
0.020 GeneticVariation BEFREE The study revealed that SLCO1B1 388 G > A occurred significantly more frequently in neonates with hyperbilirubinemia than in controls (RR = 1.50; 95% CI: 1.13-2.00). 24090270 2013
Hyperbilirubinemia
CUI: C0020433
Disease: Hyperbilirubinemia
0.020 GeneticVariation BEFREE The results suggested that Gly71Arg and Asn130Asp mutations in UGT1A1 and OATP2 genes might be involved in the development of hyperbilirubinemia in neonates. 26960716 2016