Variant: rs56059937 

    present in Gene: UGT1A3;UGT1A7;UGT1A5;UGT1A8;UGT1A9;UGT1A4;UGT1A6;UGT1A1;UGT1A10
    present in Chromosome: 2
    Position on Chromosome: 233760534
    Alleles of this Variant: T/A;C

rs56059937 in UGT1A3;UGT1A7;UGT1A5;UGT1A8;UGT1A9;UGT1A4;UGT1A6;UGT1A1;UGT1A10 gene and Gilbert Disease (disorder) PMID 11013440 2000 Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.

PMID 9627603 1998 Gilbert syndrome caused by a homozygous missense mutation (Tyr486Asp) of bilirubin UDP-glucuronosyltransferase gene.

PMID 17496722 2007 Molecular pathogenesis of Gilbert's syndrome: decreased TATA-binding protein binding affinity of UGT1A1 gene promoter.

PMID 12139570 2002 Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome.

PMID 7715297 1995 Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome.