Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs887829
rs887829
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.800 GeneticVariation GWASDB A genome-wide association study for serum bilirubin levels and gene-environment interaction in a Chinese population. 23371916

2013

dbSNP: rs887829
rs887829
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
T 0.800 GeneticVariation GWASDB Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study. 23642732

2013

dbSNP: rs887829
rs887829
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
T 0.800 GeneticVariation GWASDB Taking advantage of the lower LD and shorter haplotypes in African-ancestry populations, we identified rs887829 as a more refined proxy for the causative variant influencing bilirubin levels. 22085899

2012

dbSNP: rs887829
rs887829
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
T 0.800 GeneticVariation GWASDB Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. 19419973

2009