Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4148323
rs4148323
UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A5 ; UGT1A9 ; UGT1A4 ; UGT1A1 ; UGT1A3
CUI: C0270202
Disease: Hemolytic disease of fetus OR newborn due to ABO immunization
Hemolytic disease of fetus OR newborn due to ABO immunization 		0.010 GeneticVariation BEFREE Individuals with Gly71Arg homozygous contributed to their hyperbilirubinemia in ABO HDN patients. 31087315

2019