rs9275596, None

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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
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
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
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
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