Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10878
Gene Symbol: CFHR3
CFHR3 		0.420 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 29789
Gene Symbol: OLA1
OLA1 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 23026
Gene Symbol: MYO16
MYO16 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 259307
Gene Symbol: IL4I1
IL4I1 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 57178
Gene Symbol: ZMIZ1
ZMIZ1 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 1066
Gene Symbol: CES1
CES1 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 56981
Gene Symbol: PRDM11
PRDM11 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 203102
Gene Symbol: ADAM32
ADAM32 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 23636
Gene Symbol: NUP62
NUP62 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 5651
Gene Symbol: TMPRSS15
TMPRSS15 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 201456
Gene Symbol: FBXO15
FBXO15 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 214
Gene Symbol: ALCAM
ALCAM 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 2915
Gene Symbol: GRM5
GRM5 		0.100 GeneticVariation group GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 5054
Gene Symbol: SERPINE1
SERPINE1 		0.090 GeneticVariation group LHGDN Our data show a correlation between the 4G4G genotype of the PAI-1 gene and development of DIC in meningococcal infection. 17697137 2007
Entrez Id: 5054
Gene Symbol: SERPINE1
SERPINE1 		0.090 GeneticVariation group LHGDN The 4G/5G insertion/deletion promoter polymorphism, which leads to differences in PAI-1 production, has been demonstrated to affect the risk of developing severe complications and dying from sepsis during meningococcal infection and multiple trauma. 16237647 2005
Entrez Id: 153
Gene Symbol: ADRB1
ADRB1 		0.010 GeneticVariation group LHGDN Single nucleotide polymorphisms in genes of circulatory homeostasis in surviving pediatric intensive care patients with meningococcal infection. 18679149 2008
Entrez Id: 629
Gene Symbol: CFB
CFB 		0.010 GeneticVariation group LHGDN Activator-specific requirement of properdin in the initiation and amplification of the alternative pathway complement. 17916747 2008
Entrez Id: 118
Gene Symbol: ADD1
ADD1 		0.010 GeneticVariation group LHGDN Among patients admitted to the PICU with a meningococcal infection, the variant allele of the alpha-adducin gene was more prevalent compared with controls. 18679149 2008
Entrez Id: 10878
Gene Symbol: CFHR3
CFHR3 		0.420 GeneticVariation group GWASCAT Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 10878
Gene Symbol: CFHR3
CFHR3 		0.420 Biomarker group CTD_human Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 3075
Gene Symbol: CFH
CFH 		0.400 Biomarker group CTD_human Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010
Entrez Id: 1636
Gene Symbol: ACE
ACE 		0.320 Biomarker group CTD_human Severity of meningococcal disease in children and the angiotensin-converting enzyme insertion/deletion polymorphism. 11956052 2002
Entrez Id: 1675
Gene Symbol: CFD
CFD 		0.310 Biomarker group CTD_human Deficient alternative complement pathway activation due to factor D deficiency by 2 novel mutations in the complement factor D gene in a family with meningococcal infections. 16527897 2006
Entrez Id: 10878
Gene Symbol: CFHR3
CFHR3 		0.420 GeneticVariation group BEFREE These data may explain the association between genetic variation in both CFH and CFHR3 and susceptibility to meningococcal disease. 25534642 2014