Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs754855896
rs754855896
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011847
Disease:
Diabetes 		0.010 GeneticVariation BEFREE The aim of our study was to evaluate the frequency of the L-selectin gene T668C mutation (from thymine to cytosine at position 668) resulted in F206L an amino acid substitution in patients with overt diabetes and their unaffected first degree relatives in comparison to the unselected control population. 11064106 2000
dbSNP: rs754855896
rs754855896
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011849
Disease:
Diabetes Mellitus 		0.010 GeneticVariation BEFREE The aim of our study was to evaluate the frequency of the L-selectin gene T668C mutation (from thymine to cytosine at position 668) resulted in F206L an amino acid substitution in patients with overt diabetes and their unaffected first degree relatives in comparison to the unselected control population. 11064106 2000
dbSNP: rs754855896
rs754855896
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.010 GeneticVariation BEFREE It was also shown that there is an association between T668C mutation and low HLA related risk of IDDM development, the highest frequency of F206L mutation in the EGF domain of L-selectin was observed in relatives with 'protective' HLA DQB1*0602 allele and nonDRB1*03-nonDRB1*04 haplotype, while in subjects with highest risk of IDDM haplotype the frequency of T668C mutation was similar to the controls. 11064106 2000
dbSNP: rs1573649
rs1573649
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs2051549
rs2051549
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs2051549
rs2051549
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0026769
Disease:
Multiple Sclerosis 		0.700 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
dbSNP: rs2071550
rs2071550
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs2301271
rs2301271
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs6902723
rs6902723
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0026769
Disease:
Multiple Sclerosis 		0.700 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
dbSNP: rs6903130
rs6903130
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0026769
Disease:
Multiple Sclerosis 		0.700 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
dbSNP: rs6903130
rs6903130
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs7453920
rs7453920
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs7453920
rs7453920
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0026769
Disease:
Multiple Sclerosis 		0.700 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
dbSNP: rs7756516
rs7756516
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent 		0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
dbSNP: rs7756516
rs7756516
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836 2007
dbSNP: rs7768538
rs7768538
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0026769
Disease:
Multiple Sclerosis 		0.700 GeneticVariation GWASDB Risk alleles for multiple sclerosis identified by a genomewide study. 17660530 2007
dbSNP: rs7774954
rs7774954
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0003873
Disease:
Rheumatoid Arthritis 		0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836 2007
dbSNP: rs6902723
rs6902723
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs6903130
rs6903130
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs7756516
rs7756516
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
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: rs7769979
rs7769979
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		0.010 GeneticVariation BEFREE Sequential removal of SLE-associated DRB1 haplotypes revealed independent effects due to variation within OR2H2 (extended class I, rs362521, p = 0.006), CREBL1 (class III, rs8283, p = 0.01), and DQB2 (class II, rs7769979, p = 0.003, and rs10947345, p = 0.0004). 19851445 2009
dbSNP: rs7774954
rs7774954
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0036421
Disease:
Systemic Scleroderma 		0.700 GeneticVariation GWASDB Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. 20383147 2010
dbSNP: rs7453920
rs7453920
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0019163
Disease:
Hepatitis B 		G 0.880 GeneticVariation GWASCAT A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population. 21750111 2011
dbSNP: rs7453920
rs7453920
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0019163
Disease:
Hepatitis B 		G 0.880 GeneticVariation GWASDB A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population. 21750111 2011
dbSNP: rs2301271
rs2301271
Entrez Id: 3120
Gene Symbol: HLA-DQB2
HLA-DQB2
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		T 0.800 GeneticVariation GWASCAT Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. 21408207 2011