Review eQTL and phenotype association data in this region using PheGenI
EBI GWAS Catalog
Description |
A genome-wide assessment of variability in human serum metabolism. |
A genome-wide association study for serum bilirubin levels and gene-environment interaction in a Chinese population. |
A genome-wide association study identifies UGT1A1 as a regulator of serum cell-free DNA in young adults: The Cardiovascular Risk in Young Finns Study. |
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. |
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. |
An atlas of genetic influences on human blood metabolites. |
Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study. |
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. |
Discovery and refinement of loci associated with lipid levels. |
Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. |
Genetic determinants influencing human serum metabolome among African Americans. |
Genome-wide analysis of hepatic lipid content in extreme obesity. |
Genome-wide association meta-analysis for total serum bilirubin levels. |
Genome-wide association of serum bilirubin levels in Korean population. |
Genome-wide association study identifies multiple loci associated with bladder cancer risk. |
Human metabolic individuality in biomedical and pharmaceutical research. |
Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. |
UGT1A1 is a major locus influencing bilirubin levels in African Americans. |