rs2306283, SLCO1B1

N. diseases: 16
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 results suggested that Gly71Arg and Asn130Asp mutations in UGT1A1 and OATP2 genes might be involved in the development of hyperbilirubinemia in neonates. 26960716 2016
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