rs3918242, MMP9

N. diseases: 54
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Centriacinar Emphysema
CUI: C0221227
Disease: Centriacinar Emphysema
0.010 GeneticVariation BEFREE The TGFB1 rs2241718 and MMP9 rs3918242 SNPs were associated with centrilobular emphysema (p = 0.022 and p = 0.008), and the TNF rs1800629 SNP with paraseptal emphysema (p = 0.017). 23734748 2013