Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia. 23099197 2013
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias. 23992562 2013
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Crigler-Najjar syndrome in The Netherlands: identification of four novel UGT1A1 alleles, genotype-phenotype correlation, and functional analysis of 10 missense mutants. 19830808 2010
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Influence of mutations associated with Gilbert and Crigler-Najjar type II syndromes on the glucuronidation kinetics of bilirubin and other UDP-glucuronosyltransferase 1A substrates. 18004206 2007
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia. 17229650 2007
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Spectrum of UGT1A1 mutations in Crigler-Najjar (CN) syndrome patients: identification of twelve novel alleles and genotype-phenotype correlation. 15712364 2005
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Rapid proteasomal degradation of translocation-deficient UDP-glucuronosyltransferase 1A1 proteins in patients with Crigler-Najjar type II. 14550264 2003
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Association of a homozygous (TA)8 promoter polymorphism and a N400D mutation of UGT1A1 in a child with Crigler-Najjar type II syndrome. 12402338 2002
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus. 11370628 2001
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype. 11013440 2000
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Analysis of bilirubin uridine 5'-diphosphate (UDP)-glucuronosyltransferase gene mutations in seven patients with Crigler-Najjar syndrome type II. 9621515 1998
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease. 9639672 1998
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP-glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler-Najjar type II. 8706880 1996
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase. 7989595 1994
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Identification of an A-to-G missense mutation in exon 2 of the UGT1 gene complex that causes Crigler-Najjar syndrome type 2. 8276413 1993
dbSNP: rs397978903
rs397978903
Entrez Id: 54575;54576;54577;54578;54579;54600;54657;54658;54659
Gene Symbol: UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
UGT1A10;UGT1A8;UGT1A7;UGT1A6;UGT1A5;UGT1A9;UGT1A4;UGT1A1;UGT1A3
CUI: C2931132
Disease:
Crigler Najjar syndrome, type 2
0.700 GeneticVariation UNIPROT Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II. 8280139 1993