rs9275596, None

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Idiopathic Membranous Glomerulonephritis
0.010 GeneticVariation BEFREE Conditional logistic regression analysis displayed that SNPs protective from IMN (odds ratio < 1.00) were still significantly associated with IMN (p = 3.67E-4 for rs660895 and p = 1.26E-4 for rs9275224) with the most significant SNP rs9275596 as a covariate. 28929317 2017
IgE-mediated food allergy
CUI: C4554344
Disease: IgE-mediated food allergy
0.010 GeneticVariation BEFREE Here we conduct the first genome-wide association study of well-defined FA, including specific subtypes (peanut, milk and egg) in 2,759 US participants (1,315 children and 1,444 parents) from the Chicago Food Allergy Study, and identify peanut allergy (PA)-specific loci in the HLA-DR and -DQ gene region at 6p21.32, tagged by rs7192 (P=5.5 × 10(-8)) and rs9275596 (P=6.8 × 10(-10)), in 2,197 participants of European ancestry. 25710614 2015
Allergy to peanuts
CUI: C0559470
Disease: Allergy to peanuts
0.020 GeneticVariation BEFREE Here we conduct the first genome-wide association study of well-defined FA, including specific subtypes (peanut, milk and egg) in 2,759 US participants (1,315 children and 1,444 parents) from the Chicago Food Allergy Study, and identify peanut allergy (PA)-specific loci in the HLA-DR and -DQ gene region at 6p21.32, tagged by rs7192 (P=5.5 × 10(-8)) and rs9275596 (P=6.8 × 10(-10)), in 2,197 participants of European ancestry. 25710614 2015
Allergy to peanuts
CUI: C0559470
Disease: Allergy to peanuts
0.020 GeneticVariation BEFREE However, a recent large genomewide association study of patients with peanut allergy and their family members found 2 PA-associated single-nucleotide polymorphisms (rs9275596 and rs7192) mapping to regions involving the HLA-DR and HLA-DQ genes. 26522257 2015
Rheumatoid Arthritis
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
Diabetes Mellitus, Insulin-Dependent
0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545 2007
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
0.720 GeneticVariation BEFREE After Cochran-Armitage test for trend analysis, seven IgAN-associated SNPs located in the major histocompatibility complex (MHC) region were found to be significantly associated with the susceptibility of IMN, with rs9275596 as the top one (p = 1.97E-43, OR = 3.977). 28929317 2017
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
0.720 GeneticVariation BEFREE The T allele at rs9275596 was significantly associated with macroscopic haematuria of IgAN patients under the dominant and additive models of inheritance, (P < 0.001, Pc = 0.007, OR = 2.983) and (P < 0.001, Pc = 0.007, OR = 2.17), respectively. 27450519 2017
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
0.720 GeneticVariation BEFREE A combination of the rs2856717T/C, rs9275596C/T, and rs2412971A/G had effects on the susceptibility of IgAN (P = 0.001). 27450519 2017
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
0.720 GeneticVariation GWASCAT Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. 25305756 2014
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
0.800 GeneticVariation GWASCAT Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633 2011
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
0.800 GeneticVariation GWASDB Genome-wide association study identifies susceptibility loci for IgA nephropathy. 21399633 2011