Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3891175
rs3891175
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C1527304
Disease:
Allergic Reaction
T 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569 2013
dbSNP: rs3189152
rs3189152
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0019163
Disease:
Hepatitis B
0.700 GeneticVariation GWASDB A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. 23760081 2013
dbSNP: rs1063355
rs1063355
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0010346
Disease:
Crohn Disease
0.700 GeneticVariation GWASDB A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. 23266558 2013
dbSNP: rs201386475
rs201386475
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761 2011
dbSNP: rs3828800
rs3828800
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761 2011
dbSNP: rs3891175
rs3891175
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761 2011
dbSNP: rs2854275
rs2854275
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0149678
Disease:
Epstein-Barr Virus Infections
T 0.800 GeneticVariation GWASCAT A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). 23326239 2013
dbSNP: rs2854275
rs2854275
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0149678
Disease:
Epstein-Barr Virus Infections
T 0.800 GeneticVariation GWASDB A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). 23326239 2013
dbSNP: rs2854275
rs2854275
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0201278
Disease:
Antibody measurement (procedure)
T 0.700 GeneticVariation GWASCAT A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). 23326239 2013
dbSNP: rs9274614
rs9274614
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0024301
Disease:
Lymphoma, Follicular
0.700 GeneticVariation GWASDB A meta-analysis of genome-wide association studies of follicular lymphoma. 23025665 2012
dbSNP: rs1140343
rs1140343
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0403396
Disease:
Steroid-sensitive nephrotic syndrome
0.010 GeneticVariation BEFREE Four common single nucleotide polymorphisms (SNPs) in HLA-DQA1 and HLA-DQB1 (rs1129740, rs9273349, rs1071630, and rs1140343) were significantly associated with SSNS at or near the Bonferroni-adjusted P value for the number of single variants that were tested (odds ratio, 2.11; 95% confidence interval, 1.56 to 2.86; P=1.68×10(-6) (Fisher exact test). 25349203 2015
dbSNP: rs1063355
rs1063355
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0242383
Disease:
Age related macular degeneration
0.010 GeneticVariation BEFREE Four of 12 miRNAs significantly elevated in AAMD retina (hsa-miR-155-5p, hsa-let-7a-5p, hsa-let-7b-5p hsa-let-7d-5p) also showed strong pairing capacity (TarBase 7.1 context++ score <-0.2, miRanda 3.3 pairing score >150) with miRNA target transcripts encoded by AAMD-associated SNPs resident in HLA-DQB1 (rs1063355, hsa-miR-155-5p) and TGFBR1 (rs868, hsa-let-7). 28343170 2017
dbSNP: rs1130399
rs1130399
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C1270972
Disease:
Mild cognitive disorder
0.010 GeneticVariation BEFREE Furthermore, we detected the above four associations in mild cognitive impairment (MCI) sub-group analysis, and two risk loci (rs35445101 and rs1130399) were also the smaller baseline volume of the left posterior cingulate in (NC) sub-group analysis. 27056075 2017
dbSNP: rs201184533
rs201184533
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0004096
Disease:
Asthma
C 0.700 GeneticVariation GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019
dbSNP: rs3891175
rs3891175
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0241910
Disease:
Autoimmune Chronic Hepatitis
0.700 GeneticVariation GWASCAT Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. 28779025 2018
dbSNP: rs3891175
rs3891175
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0008313
Disease:
Cholangitis, Sclerosing
0.700 GeneticVariation GWASCAT Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. 28779025 2018
dbSNP: rs3891175
rs3891175
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C1332355
Disease:
Autoimmune Hepatitis with Centrilobular Necrosis
0.700 GeneticVariation GWASCAT Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. 28779025 2018
dbSNP: rs9273542
rs9273542
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0027726
Disease:
Nephrotic Syndrome
T 0.700 GeneticVariation GWASCAT Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. 31263063 2019
dbSNP: rs9273404
rs9273404
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease
G 0.700 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561 2019
dbSNP: rs9274407
rs9274407
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C2239176
Disease:
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368 2013
dbSNP: rs28724231
rs28724231
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0003872
Disease:
Arthritis, Psoriatic
0.700 GeneticVariation GWASCAT Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis. 30552173 2019
dbSNP: rs9274477
rs9274477
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0027404
Disease:
Narcolepsy
G 0.700 GeneticVariation GWASCAT Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. 24204295 2013
dbSNP: rs9274477
rs9274477
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0751362
Disease:
Narcolepsy-Cataplexy Syndrome
G 0.700 GeneticVariation GWASCAT Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. 24204295 2013
dbSNP: rs114544105
rs114544105
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0016529
Disease:
Forced expiratory volume function
A 0.700 GeneticVariation GWASCAT Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. 28166213 2017
dbSNP: rs1063355
rs1063355
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
T 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. 30054458 2018