CFH, complement factor H, 3075

N. diseases: 393; N. variants: 150
Disease: Myeloperoxidase Measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C2698399
Disease:
Myeloperoxidase Measurement 		A 0.800 GeneticVariation GWASDB A locus on chromosome 1q31.1 containing the complement factor H (CFH) gene was strongly associated with serum MPO levels in 9305 subjects of European ancestry (lead SNP rs800292; P = 4.89 × 10(-41)) and in 1690 AA subjects (rs505102; P = 1.05 × 10(-8)). 23620142 2013
dbSNP: rs800292
rs800292
Entrez Id: 3075
Gene Symbol: CFH
CFH
CUI: C2698399
Disease:
Myeloperoxidase Measurement 		A 0.800 GeneticVariation GWASCAT A locus on chromosome 1q31.1 containing the complement factor H (CFH) gene was strongly associated with serum MPO levels in 9305 subjects of European ancestry (lead SNP rs800292; P = 4.89 × 10(-41)) and in 1690 AA subjects (rs505102; P = 1.05 × 10(-8)). 23620142 2013