Source: GWASDB ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64241
Gene Symbol: ABCG8
ABCG8 		0.200 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 54578
Gene Symbol: UGT1A6
UGT1A6 		0.180 GeneticVariation disease GWASDB A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. 22558097 2012
Entrez Id: 54657
Gene Symbol: UGT1A4
UGT1A4 		0.180 GeneticVariation disease GWASDB A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. 22558097 2012
Entrez Id: 54575
Gene Symbol: UGT1A10
UGT1A10 		0.180 GeneticVariation disease GWASDB A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. 22558097 2012
Entrez Id: 54577
Gene Symbol: UGT1A7
UGT1A7 		0.180 GeneticVariation disease GWASDB A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. 22558097 2012
Entrez Id: 54576
Gene Symbol: UGT1A8
UGT1A8 		0.180 GeneticVariation disease GWASDB A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. 22558097 2012
Entrez Id: 54600
Gene Symbol: UGT1A9
UGT1A9 		0.140 GeneticVariation disease GWASDB A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. 22558097 2012
Entrez Id: 54579
Gene Symbol: UGT1A5
UGT1A5 		0.140 GeneticVariation disease GWASDB A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. 22558097 2012
Entrez Id: 54659
Gene Symbol: UGT1A3
UGT1A3 		0.140 GeneticVariation disease GWASDB A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. 22558097 2012
Entrez Id: 23673
Gene Symbol: STX12
STX12 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 3371
Gene Symbol: TNC
TNC 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 9630
Gene Symbol: GNA14
GNA14 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 29994
Gene Symbol: BAZ2B
BAZ2B 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 7576
Gene Symbol: ZNF28
ZNF28 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 1602
Gene Symbol: DACH1
DACH1 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 55691
Gene Symbol: FRMD4A
FRMD4A 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 50514
Gene Symbol: DELEC1
DELEC1 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 85461
Gene Symbol: TANC1
TANC1 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 348645
Gene Symbol: C22orf34
C22orf34 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 283953
Gene Symbol: TMEM114
TMEM114 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 4651
Gene Symbol: MYO10
MYO10 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 137868
Gene Symbol: SGCZ
SGCZ 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 91316
Gene Symbol: GUSBP11
GUSBP11 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 83872
Gene Symbol: HMCN1
HMCN1 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
Entrez Id: 84665
Gene Symbol: MYPN
MYPN 		0.100 GeneticVariation disease GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007