Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1335532
rs1335532
CD58
0.810 GeneticVariation BEFREE In summary, our results suggest that ASCL2 mediates the protective function of rs1335532 minor (C) allele in MS. 30006149

2018
dbSNP: rs1335532
rs1335532
CD58
A 0.810 GeneticVariation GWASDB No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. 24234648

2014
dbSNP: rs1335532
rs1335532
CD58
A 0.810 GeneticVariation GWASDB Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs1335532
rs1335532
CD58
A 0.810 GeneticVariation GWASCAT Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. 21833088

2011
dbSNP: rs1335532
rs1335532
CD58
0.810 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364

2011
dbSNP: rs1335532
rs1335532
CD58
A 0.810 GeneticVariation GWASDB Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. 19525955

2009
dbSNP: rs1335532
rs1335532
CD58
A 0.810 GeneticVariation GWASCAT Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. 19525955

2009