Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2454138
rs2454138
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0026769
Disease:
Multiple Sclerosis
A 0.700 GeneticVariation GWASCAT Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials. 29521573 2019
dbSNP: rs615672
rs615672
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0026769
Disease:
Multiple Sclerosis
0.700 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
dbSNP: rs9270986
rs9270986
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0026769
Disease:
Multiple Sclerosis
0.700 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
dbSNP: rs660895
rs660895
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0026769
Disease:
Multiple Sclerosis
0.010 GeneticVariation BEFREE Using a logistic regression model, two SNPs (MHC Class III SNP rs422951 in the NOTCH4 gene and MHC Class II SNP rs3997849, susceptible alleles A and G, respectively) were independently associated with MS susceptibility (204 patients; 280 controls), two (MHC Class II SNP rs660895 and MHC Class I SNP rs2269704 in the NRM gene, susceptible alleles G and G, respectively) with aquaporin-4- (AQP4-) MS susceptibility (149 patients; 280 controls) and a single SNP (MHC Class II SNP rs1694112, susceptible allele G) was significant when contrasting AQP4+ against AQP4- patients. 21654846 2011
dbSNP: rs17879469
rs17879469
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
CUI: C0026769
Disease:
Multiple Sclerosis
0.010 GeneticVariation BEFREE There were no significant (P<0.05) associations between the A49G genotype and risk of MS, either before or after stratification for presence of the DR15 haplotype. 18378005 2008