Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs426736
rs426736
CFHR3
0.800 GeneticVariation GWASCAT Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs426736
rs426736
CFHR3
0.800 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs10749071
rs10749071 		0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs10838427
rs10838427
PRDM11
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs11728925
rs11728925 		0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs1299491
rs1299491
NUP62 ; IL4I1
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs13070790
rs13070790
ALCAM
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs1749824
rs1749824
ZMIZ1
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs1792624
rs1792624 		0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs2244614
rs2244614
CES1
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs2406176
rs2406176
TMPRSS15
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs2420864
rs2420864
CNTNAP5
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs4556879
rs4556879
FBXO15
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs4809944
rs4809944 		0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs4897668
rs4897668 		0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs4972431
rs4972431
OLA1
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs4976846
rs4976846
MYO16 ; MYO16-AS1
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs655683
rs655683
GRM5
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs7830326
rs7830326
ADAM32
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013

2010
dbSNP: rs4986790
rs4986790
TLR4
0.030 GeneticVariation BEFREE We could not observe a significant influence of CD14 C-159T and TLR4 Asp299Gly polymorphisms on the risk of developing IMD in surviving meningococcal disease patients. 19809507

2009
dbSNP: rs4986790
rs4986790
TLR4
0.030 GeneticVariation BEFREE We investigated an association between 2 TLR4 mutations (Asp(299)Gly and Thr(399)Ile) and meningococcal disease in 197 patients and 214 healthy controls by allele-specific real time polymerase chain reaction and direct sequencing. 16395111

2006
dbSNP: rs4986790
rs4986790
TLR4
0.030 GeneticVariation BEFREE The allele frequency of the Asp299Gly polymorphism was 5.9% among 879 blood donors, 6.5% among 1047 patients with microbiologically proven meningococcal disease, and 4.1% among 86 patients who died of meningococcal disease. 11494169

2001
dbSNP: rs11913168
rs11913168 		0.010 GeneticVariation BEFREE We identified two new polymorphisms, rs4823231 and rs11913168, showing signs of association with meningococcal disease susceptibility. 31061469

2019
dbSNP: rs4823231
rs4823231
ATXN10
0.010 GeneticVariation BEFREE We identified two new polymorphisms, rs4823231 and rs11913168, showing signs of association with meningococcal disease susceptibility. 31061469

2019
dbSNP: rs1065489
rs1065489
CFH
0.010 GeneticVariation BEFREE Theoretical predictions point to a functional effect of rs1065489, which may be directly responsible for protection against MD.</span> 27805046

2016