Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2073244
rs2073244
PAX9 ; LOC105370455
0.010 GeneticVariation BEFREE The AG and GG genotypes at rs2073244 and the CC genotype at rs4904210, with interaction coefficients greater than unity suggest that they may strengthen the association between HCMV infection and LBW. 26333297

2016
dbSNP: rs352139
rs352139
TLR9
0.010 GeneticVariation BEFREE The rs352139 GG genotype showed a significantly reduced relative risk for HCMV infection (Pc = 0.006). 27105145

2016
dbSNP: rs3761548
rs3761548
FOXP3
0.010 GeneticVariation BEFREE In conclusion, this is the first report on FOXP3 rs3761548 SNP in allo-HSCT and we suggest that this SNP be considered a candidate marker for predicting the development of HVOD and CMV infection after allo-HSCT. 26735609

2016
dbSNP: rs4904210
rs4904210
PAX9
0.010 GeneticVariation BEFREE The AG and GG genotypes at rs2073244 and the CC genotype at rs4904210, with interaction coefficients greater than unity suggest that they may strengthen the association between HCMV infection and LBW. 26333297

2016
dbSNP: rs231775
rs231775
CTLA4
0.010 GeneticVariation BEFREE An almost three-fold increased risk was observed for the incidence of symptomatic HCMV infection in mutant genotype carriers of rs231775 and rs3087243 SNPs under additive and recessive models, respectively. 25356901

2015
dbSNP: rs3087243
rs3087243
CTLA4
0.010 GeneticVariation BEFREE In the present study, we have made an attempt to investigate the impact of CTLA4 single nucleotide polymorphisms (SNPs) (rs231775, rs5742909, rs11571317, rs16840252, rs4553808, rs3087243) and dinucleotide (AT)n repeat polymorphism on the incidence of symptomatic HCMV infection (disease) among 270 renal allograft recipients. 25356901

2015
dbSNP: rs121917864
rs121917864
TLR2
0.010 GeneticVariation BEFREE Relationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection. 24813591

2014
dbSNP: rs4986790
rs4986790
TLR4
0.010 GeneticVariation BEFREE Relationship between toll-like receptor 2 Arg677Trp and Arg753Gln and toll-like receptor 4 Asp299Gly polymorphisms and cytomegalovirus infection. 24813591

2014
dbSNP: rs76838169
rs76838169
GJB2
0.010 GeneticVariation BEFREE Mutations 79G>A, 109G>A, 341A>G, and 608T>C were found in neonates with and without CMV infection. 23665763

2013
dbSNP: rs1061680
rs1061680
LILRB1
0.010 GeneticVariation BEFREE The LILRB1 I142T polymorphism was associated with both CMV disease and low nadir CD4(+) T cell counts in Caucasians, but the clearest determinant of low nadir CD4(+) T cell count in African American patients was DARC T-46C. 22154842

2012
dbSNP: rs374465594
rs374465594
IL2
0.010 GeneticVariation BEFREE The LILRB1 I142T polymorphism was associated with both CMV disease and low nadir CD4(+) T cell counts in Caucasians, but the clearest determinant of low nadir CD4(+) T cell count in African American patients was DARC T-46C. 22154842

2012