rs1060500764, SMAD3

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fibrosis, Liver
CUI: C0239946
Disease: Fibrosis, Liver
0.010 GeneticVariation BEFREE Overexpression of HNRNPA1 (or its T51A mutant) in HSCs of mice inhibited liver fibrosis. 26435271 2016