Source: CURATED

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16851720
rs16851720
RNF7
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		C 0.810 GeneticVariation GWASDB Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012
dbSNP: rs16851720
rs16851720
RNF7
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		C 0.810 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012
dbSNP: rs4374383
rs4374383
MERTK
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		A 0.810 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012
dbSNP: rs4374383
rs4374383
MERTK
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		A 0.810 GeneticVariation GWASDB Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012
dbSNP: rs2629751
rs2629751
GLT8D2
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		G 0.800 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012
dbSNP: rs2629751
rs2629751
GLT8D2
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012
dbSNP: rs9380516
rs9380516
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		T 0.800 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012
dbSNP: rs9380516
rs9380516
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		T 0.800 GeneticVariation GWASDB Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784

2012
dbSNP: rs1227756
rs1227756
COL13A1
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010
dbSNP: rs1396171148
rs1396171148
FARSB
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1419129874
rs1419129874
FARSB
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1466642025
rs1466642025
FARSB
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1553553086
rs1553553086
FARSB
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1553554543
rs1553554543
FARSB
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		C 0.700 CausalMutation CLINVAR

dbSNP: rs2645424
rs2645424
FDFT1
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010
dbSNP: rs2710833
rs2710833
DDX60L ; LOC107986198
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010
dbSNP: rs2896019
rs2896019
PNPLA3
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		G 0.700 GeneticVariation GWASCAT Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan. 23535911

2013
dbSNP: rs343064
rs343064
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010
dbSNP: rs367956522
rs367956522
ATP7B
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		C 0.700 CausalMutation CLINVAR

dbSNP: rs643608
rs643608
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010
dbSNP: rs6487679
rs6487679
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010
dbSNP: rs6591182
rs6591182
EHBP1L1
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010
dbSNP: rs757075712
rs757075712
TFAM
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs887304
rs887304
CRACR2A
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. 20708005

2010