Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1898830
rs1898830
TLR2
0.020 GeneticVariation BEFREE Polymorphisms of the TLR2 (rs3804100, rs1898830), TLR4 (rs4986791), and TLR9 (rs352140) were shown to have a role in congenital CMV infection. 27586547

2016
dbSNP: rs3804100
rs3804100
TLR2
0.020 GeneticVariation BEFREE Polymorphisms of the TLR2 (rs3804100, rs1898830), TLR4 (rs4986791), and TLR9 (rs352140) were shown to have a role in congenital CMV infection. 27586547

2016
dbSNP: rs1898830
rs1898830
TLR2
0.020 GeneticVariation BEFREE Furthermore, the AG genotype at SNP rs1898830 in the TLR-2 gene tended to be identified less frequently in children with congenital CMV infection. 23906542

2013
dbSNP: rs3804100
rs3804100
TLR2
0.020 GeneticVariation BEFREE The CC genotype at SNP rs3804100 in the TLR-2 gene was significantly associated with congenital CMV infection but not with congenital CMV disease. 23906542

2013
dbSNP: rs333
rs333
CCR5 ; CCR5AS
0.010 GeneticVariation BEFREE A panel of 11 candidate single nucleotide polymorphisms (SNPs): TNF rs1799964, TNF rs1800629, TNFRSF1A rs4149570, IL1B rs16944, IL1B rs1143634, IL10 rs1800896, IL10RA rs4252279, IL12B rs3212227, CCL2 rs1024611, CCL2 rs13900, CCR5 rs333 was genotyped in 470 infants (72 with confirmed intrauterine CMV infection and 398 uninfected controls), and related to congenital CMV infection, and the outcome. 28501927

2017
dbSNP: rs352140
rs352140
TLR9
0.010 GeneticVariation BEFREE Polymorphisms of the TLR2 (rs3804100, rs1898830), TLR4 (rs4986791), and TLR9 (rs352140) were shown to have a role in congenital CMV infection. 27586547

2016
dbSNP: rs4986791
rs4986791
TLR4
0.010 GeneticVariation BEFREE Polymorphisms of the TLR2 (rs3804100, rs1898830), TLR4 (rs4986791), and TLR9 (rs352140) were shown to have a role in congenital CMV infection. 27586547

2016
dbSNP: rs2255336
rs2255336
KLRK1 ; KLRC4-KLRK1 ; LOC101928100
0.010 GeneticVariation BEFREE A Thr72Ala polymorphism in the NKG2D gene is associated with early symptomatic congenital cytomegalovirus disease. 25861030

2015
dbSNP: rs72558132
rs72558132
HLA-B ; HLA-C
0.010 GeneticVariation BEFREE A Thr72Ala polymorphism in the NKG2D gene is associated with early symptomatic congenital cytomegalovirus disease. 25861030

2015