Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9523762
rs9523762
0.820 GeneticVariation BEFREE In a subgroup analysis, rs1411751 was found to be associated with NMO (OR=0.36, P(corr)=0.03), and rs9523762 was marginally associated with both NMO and MS. 24135429

2013

dbSNP: rs9523762
rs9523762
0.820 GeneticVariation BEFREE Only rs9523762 mapping in the GPC5 gene was significantly associated (G allele, P=1.6 × 10(-5); odds ratio (95% confidence interval)=1.23 (1.12-1.36)), supporting a role for this proteoglycan in MS predisposition. 20944657

2011

dbSNP: rs9523762
rs9523762
0.820 GeneticVariation GWASDB Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. 19010793

2009

dbSNP: rs9523762
rs9523762
0.820 GeneticVariation GWASCAT Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. 19010793

2009