IRF2, interferon regulatory factor 2, 3660

N. diseases: 86; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3775578
rs3775578
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0869220
Disease:
Adverse effects, not elsewhere classified
C 0.700 GeneticVariation GWASCAT Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. 30420678 2019
dbSNP: rs17488073
rs17488073
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0002395
Disease:
Alzheimer's Disease
G 0.700 GeneticVariation GWASCAT Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. 29274321 2018
dbSNP: rs890195
rs890195
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs890195
rs890195
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis
0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs3733475
rs3733475
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE Five SNPs, rs3733475A/C (IRF2), rs2069832A/G (IL6), rs2012075G/A (IFNGR2) and rs1400656G/A (STAT4) and rs1805011C/A (IL4RA) were found to be associated with asthma in family based as well as in case-control analyses (P=0.002, P=0.001, P=0.004, P=0.003 and P=0.001, respectively). 25994869 2015
dbSNP: rs13146124
rs13146124
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE When the association was analyzed in 834 Japanese patients with SLE and 817 healthy controls, rs13146124 T was significantly increased in SLE compared with healthy controls (dominant model, P = 5.4×10(-4), Bonferroni-corrected P [Pc] = 0.026, odds ratio [OR] 1.48, 95% confidence interval [CI] 1.18-1.85). 25285625 2014
dbSNP: rs13139310
rs13139310
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0019348
Disease:
Herpes Simplex Infections
0.010 GeneticVariation BEFREE Eight IRF2 SNPs were significantly associated with IFN-γ production after herpes simplex virus (HSV) stimulation (P = 0.048-0.0008), including an AD-associated SNP (rs13139310, P = 0.008). 22113474 2012
dbSNP: rs13139310
rs13139310
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0011615
Disease:
Dermatitis, Atopic
0.010 GeneticVariation BEFREE Eight IRF2 SNPs were significantly associated with IFN-γ production after herpes simplex virus (HSV) stimulation (P = 0.048-0.0008), including an AD-associated SNP (rs13139310, P = 0.008). 22113474 2012
dbSNP: rs13139310
rs13139310
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0013595
Disease:
Eczema
0.010 GeneticVariation BEFREE Eight IRF2 SNPs were significantly associated with IFN-γ production after herpes simplex virus (HSV) stimulation (P = 0.048-0.0008), including an AD-associated SNP (rs13139310, P = 0.008). 22113474 2012
dbSNP: rs3756094
rs3756094
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0013595
Disease:
Eczema
0.010 GeneticVariation BEFREE Significant associations were observed between AD and two SNPs (rs793814, P = 0.007, odds ratio (OR) = 0.52; rs3756094, P = 0.037, OR = 0.66) among European Americans and one SNP (rs3775572, P = 0.016, OR = 0.46) among African Americans. 22113474 2012
dbSNP: rs3756094
rs3756094
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0011615
Disease:
Dermatitis, Atopic
0.010 GeneticVariation BEFREE Significant associations were observed between AD and two SNPs (rs793814, P = 0.007, odds ratio (OR) = 0.52; rs3756094, P = 0.037, OR = 0.66) among European Americans and one SNP (rs3775572, P = 0.016, OR = 0.46) among African Americans. 22113474 2012
dbSNP: rs3775572
rs3775572
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0011615
Disease:
Dermatitis, Atopic
0.010 GeneticVariation BEFREE Significant associations were observed between AD and two SNPs (rs793814, P = 0.007, odds ratio (OR) = 0.52; rs3756094, P = 0.037, OR = 0.66) among European Americans and one SNP (rs3775572, P = 0.016, OR = 0.46) among African Americans. 22113474 2012
dbSNP: rs3775572
rs3775572
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0013595
Disease:
Eczema
0.010 GeneticVariation BEFREE Significant associations were observed between AD and two SNPs (rs793814, P = 0.007, odds ratio (OR) = 0.52; rs3756094, P = 0.037, OR = 0.66) among European Americans and one SNP (rs3775572, P = 0.016, OR = 0.46) among African Americans. 22113474 2012
dbSNP: rs793814
rs793814
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0013595
Disease:
Eczema
0.010 GeneticVariation BEFREE Significant associations were observed between AD and two SNPs (rs793814, P = 0.007, odds ratio (OR) = 0.52; rs3756094, P = 0.037, OR = 0.66) among European Americans and one SNP (rs3775572, P = 0.016, OR = 0.46) among African Americans. 22113474 2012
dbSNP: rs793814
rs793814
Entrez Id: 3660
Gene Symbol: IRF2
IRF2
CUI: C0011615
Disease:
Dermatitis, Atopic
0.010 GeneticVariation BEFREE Significant associations were observed between AD and two SNPs (rs793814, P = 0.007, odds ratio (OR) = 0.52; rs3756094, P = 0.037, OR = 0.66) among European Americans and one SNP (rs3775572, P = 0.016, OR = 0.46) among African Americans. 22113474 2012