Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2420864
rs2420864
Entrez Id: 129684
Gene Symbol: CNTNAP5
CNTNAP5
CUI: C0025303
Disease:
Meningococcal Infections
0.700 GeneticVariation GWASDB Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. 20694013 2010