Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113090017
rs113090017
NR1H4
0.010 GeneticVariation BEFREE Heterozygous termination codon mutation of NR1H4 R176X was found in idiopathic infantile cholestasis. 21633855

2012