rs12252, IFITM3

N. diseases: 23
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
0.040 GeneticVariation BEFREE The IFITM3 allele (rs12252-C) was suggested as a population-based genetic risk factor for severe influenza virus infection by A(H1N1)pdm09. 28842783 2018
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
0.040 GeneticVariation BEFREE <i>IFITM3</i> rs12252-C was associated with severe influenza virus infection in several studies, however whether this association is universal to all types of influenza virus or diverse ethnic populations remain controversial. 28713779 2017
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
0.040 GeneticVariation BEFREE Our meta-analysis suggests that IFITM3 rs12252 T>C polymorphism is significantly associated with increased risk of severe influenza but not with the chance of initial virus infection. 25778715 2015
Virus Diseases
CUI: C0042769
Disease: Virus Diseases
0.040 GeneticVariation BEFREE The SNP rs12252-C allele alters the function of interferon-induced transmembrane protein-3 increasing the disease severity of influenza virus infection in Caucasians, but the allele is rare. 23361009 2013