Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9274407
rs9274407
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C4277682
Disease:
Chemical and Drug Induced Liver Injury
0.800 GeneticVariation GWASCAT Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles. 21570397 2011
dbSNP: rs9274407
rs9274407
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C4277682
Disease:
Chemical and Drug Induced Liver Injury
0.800 GeneticVariation GWASDB Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles. 21570397 2011
dbSNP: rs1770
rs1770
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.710 GeneticVariation BEFREE We identified four T1D risk loci reaching genome-wide significance in the Chinese Han population, including two novel loci, rs4320356 near <i>BTN3A1</i> (odds ratio [OR] 1.26, <i>P</i> = 2.70 × 10<sup>-8</sup>) and rs3802604 in <i>GATA3</i> (OR 1.24, <i>P</i> = 2.06 × 10<sup>-8</sup>), and two previously reported loci, rs1770 in MHC (OR 4.28, <i>P</i> = 2.25 × 10<sup>-232</sup>) and rs705699 in <i>SUOX</i> (OR 1.46, <i>P</i> = 7.48 × 10<sup>-20</sup>). 31152121 2019
dbSNP: rs1063355
rs1063355
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. 19503088 2009
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: rs1063355
rs1063355
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836 2007
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: rs2515895
rs2515895
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0036202
Disease:
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805 2012
dbSNP: rs2854272
rs2854272
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0036202
Disease:
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805 2012
dbSNP: rs2854275
rs2854275
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C1269683
Disease:
Major Depressive Disorder
0.700 GeneticVariation GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474 2019
dbSNP: rs2854275
rs2854275
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0004096
Disease:
Asthma
0.700 GeneticVariation GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474 2019
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: 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: 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: 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: 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: 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: rs4988888
rs4988888
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0036202
Disease:
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805 2012
dbSNP: rs9274299
rs9274299
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0036341
Disease:
Schizophrenia
0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs9274299
rs9274299
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0008074
Disease:
Child Development Disorders, Pervasive
0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
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: 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: rs9282114
rs9282114
Entrez Id: 3119
Gene Symbol: HLA-DQB1
HLA-DQB1
CUI: C0036202
Disease:
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805 2012
dbSNP: rs1063348
rs1063348
Entrez Id: 3119;106480429
Gene Symbol: HLA-DQB1;HLA-DQB1-AS1
HLA-DQB1;HLA-DQB1-AS1
CUI: C0403396
Disease:
Steroid-sensitive nephrotic syndrome
0.010 GeneticVariation BEFREE Increased burden of risk alleles across independent loci was associated with higher odds of SSNS, with younger age of onset across all cohorts, and with increased odds of complete remission across histologies in NEPTUNE children. rs1063348 associated with decreased glomerular expression of HLA-DRB1, HLA-DRB5, and HLA-DQB1.<b>Conclusions</b> Transethnic GWAS empowered discovery of three independent risk SNPs for pediatric SSNS. 29903748 2018