rs16851720, RNF7

N. diseases: 2
Source: CURATED ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
0.810 GeneticVariation GWASDB Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784 2012
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
0.810 GeneticVariation GWASCAT Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. 22841784 2012
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
0.700 GeneticVariation GWASCAT In the combined cohort of 2342 HCV-infected patients, the SNPs rs16851720 (in the total sample) and rs4374383 (in patients who received blood transfusions) were associated with fibrosis progression (P(combined) = 8.9 × 10(-9) and 1.1 × 10(-9), respectively). 22841784 2012