Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
0.700 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178 2013
Bilirubin level result
CUI: C1287365
Disease: Bilirubin level result
0.700 GeneticVariation GWASDB Genome-wide association meta-analysis for total serum bilirubin levels. 19414484 2009
Bilirubin measurement
CUI: C0344395
Disease: Bilirubin measurement
0.700 GeneticVariation GWASDB Genome-wide association meta-analysis for total serum bilirubin levels. 19414484 2009
Crigler Najjar syndrome, type 1
CUI: C0010324
Disease: Crigler Najjar syndrome, type 1
0.010 GeneticVariation BEFREE Altogether, the data suggested that rs4148326 and rs4124874 could be introduced as informative markers for molecular diagnosis of Crigler-Najjar type 1 and 2 and Gilbert syndrome in the Iranian population. 29085579 2017
Gilbert Disease (disorder)
CUI: C0017551
Disease: Gilbert Disease (disorder)
0.010 GeneticVariation BEFREE Altogether, the data suggested that rs4148326 and rs4124874 could be introduced as informative markers for molecular diagnosis of Crigler-Najjar type 1 and 2 and Gilbert syndrome in the Iranian population. 29085579 2017
Diarrhea
CUI: C0011991
Disease: Diarrhea
0.010 GeneticVariation BEFREE Associations were found between toxicities and gene variants (P<0.05), including neutropenia with ABCB1 (rs1045642) and SLC0B3 (rs4149117 and rs7311358); and diarrhoea with CYP2C9 (rs1057910), CYP2C19 (rs3758581), UGT1A6 (rs4124874) and SLC22A1 (rs72552763). 28817838 2017
Neutropenia
CUI: C0027947
Disease: Neutropenia
0.010 GeneticVariation BEFREE Associations were found between toxicities and gene variants (P<0.05), including neutropenia with ABCB1 (rs1045642) and SLC0B3 (rs4149117 and rs7311358); and diarrhoea with CYP2C9 (rs1057910), CYP2C19 (rs3758581), UGT1A6 (rs4124874) and SLC22A1 (rs72552763). 28817838 2017
Leukopenia
CUI: C0023530
Disease: Leukopenia
0.010 GeneticVariation BEFREE Associations were found between toxicities and gene variants (P<0.05), including neutropenia with ABCB1 (rs1045642) and SLC0B3 (rs4149117 and rs7311358); and diarrhoea with CYP2C9 (rs1057910), CYP2C19 (rs3758581), UGT1A6 (rs4124874) and SLC22A1 (rs72552763). 28817838 2017