Disease: Neonatal Jaundice ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Neonatal Jaundice
CUI: C0022353
Disease: Neonatal Jaundice
0.030 GeneticVariation BEFREE Mutation of the UGT1A1 gene, glycine to arginine at codon 71 (G71R), is related to the development of neonatal jaundice in East Asian populations but the frequency of this mutation is rare among Caucasian populations. 20528217 2011
Neonatal Jaundice
CUI: C0022353
Disease: Neonatal Jaundice
0.030 GeneticVariation BEFREE The G71R mutation may account for the increased incidence of neonatal jaundice seen in Asian populations. 19325249 2009
Neonatal Jaundice
CUI: C0022353
Disease: Neonatal Jaundice
0.030 GeneticVariation BEFREE This assay is rapid and robust for screening of SNP G211A to determine if this polymorphism plays a role in causing severe neonatal jaundice in the local context. 17506482 2007