rs2306283, SLCO1B1

N. diseases: 16
Disease: Hyperbilirubinemia, Neonatal ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hyperbilirubinemia, Neonatal
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
0.020 GeneticVariation BEFREE This study demonstrated that the 388 G>A mutation of the SLCO1B1 gene is a risk factor for developing neonatal hyperbilirubinemia in Chinese neonates, but not in white, Thai, Brazilian, or Malaysian populations; the SLCO1B1 521 T>C mutation provides protection for neonatal hyperbilirubinemia in Chinese neonates, but not in white, Thai, Brazilian, or Malaysian populations. 23850112 2014
Hyperbilirubinemia, Neonatal
CUI: C0857007
Disease: Hyperbilirubinemia, Neonatal
0.020 GeneticVariation BEFREE The SLCO1B1 388 G > A variant is associated with neonatal hyperbilirubinemia in Chinese neonates. 24090270 2013