Disease: Hyperbilirubinemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1046420357
rs1046420357
Entrez Id: 28234;115072896
Gene Symbol: SLCO1B3;SLCO1B3-SLCO1B7
SLCO1B3;SLCO1B3-SLCO1B7
CUI: C0020433
Disease:
Hyperbilirubinemia 		0.010 GeneticVariation BEFREE We previously reported that maximal body weight loss (inadequate feeding) is an independent risk factor for the development of hyperbilirubinemia in breast-fed Japanese neonates, and the UGT1A1 211G>A genotype becomes a risk factor under conditions of inadequate feeding. 25391605 2015