Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
0.820 GeneticVariation GWASDB Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. 20953186 2010
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
0.820 GeneticVariation GWASCAT Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. 20953186 2010
PSORIASIS 13, SUSCEPTIBILITY TO
CUI: C3279754
Disease: PSORIASIS 13, SUSCEPTIBILITY TO
0.700 GeneticVariation UNIPROT Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. 20953186 2010
Psoriasis
CUI: C0033860
Disease: Psoriasis
0.850 GeneticVariation GWASCAT Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. 20953188 2010
Psoriasis
CUI: C0033860
Disease: Psoriasis
0.850 GeneticVariation GWASDB Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. 20953188 2010
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
0.820 GeneticVariation BEFREE A stratified analysis of our datasets including only PsA cases (1,922 cases compared to 8,037 controls, P = 4.57 × 10⁻¹² for rs33980500) suggested that TRAF3IP2 represents a shared susceptibility for PsV and PsA. 20953188 2010
Psoriasis vulgaris
CUI: C0263361
Disease: Psoriasis vulgaris
0.710 GeneticVariation BEFREE A stratified analysis of our datasets including only PsA cases (1,922 cases compared to 8,037 controls, P = 4.57 × 10⁻¹² for rs33980500) suggested that TRAF3IP2 represents a shared susceptibility for PsV and PsA. 20953188 2010
PSORIASIS 13, SUSCEPTIBILITY TO
CUI: C3279754
Disease: PSORIASIS 13, SUSCEPTIBILITY TO
0.700 GeneticVariation UNIPROT Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. 20953188 2010
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
0.820 GeneticVariation BEFREE However, the dominant PsA-associated TRAF3IP2 (Act1) gene single-nucleotide polymorphism (rs33980500) results in decreased binding of Act1 to TRAF6. 23116200 2012
Psoriasis
CUI: C0033860
Disease: Psoriasis
0.850 GeneticVariation GWASCAT Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594 2012
Psoriasis
CUI: C0033860
Disease: Psoriasis
0.850 GeneticVariation GWASDB Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. 23143594 2012
Psoriasis
CUI: C0033860
Disease: Psoriasis
0.850 GeneticVariation BEFREE In the absence of IL-17 signaling, IL-22 was the main contributor to skin inflammation, which provides a molecular mechanism for the association of Act1(D10N) with psoriasis susceptibility. 23202271 2013
Inflammatory dermatosis
CUI: C3875321
Disease: Inflammatory dermatosis
0.010 GeneticVariation BEFREE In the absence of IL-17 signaling, IL-22 was the main contributor to skin inflammation, which provides a molecular mechanism for the association of Act1(D10N) with psoriasis susceptibility. 23202271 2013
Dermatitis
CUI: C0011603
Disease: Dermatitis
0.010 GeneticVariation BEFREE In the absence of IL-17 signaling, IL-22 was the main contributor to skin inflammation, which provides a molecular mechanism for the association of Act1(D10N) with psoriasis susceptibility. 23202271 2013
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE The rs33980500 and rs13193677 resulted significantly associated with SLE susceptibility (P = 0.021, odds ratio (OR) = 1.71, and P = 0.046, OR = 1.73, respectively). 23836313 2013
Pericarditis
CUI: C0031046
Disease: Pericarditis
0.010 GeneticVariation BEFREE All three TRAF3IP2 single nucleotide polymorphisms resulted associated with the development of pericarditis; in particular, rs33980500 showed the strongest association (P = 0.002, OR 2.59). 23836313 2013
Psoriasis
CUI: C0033860
Disease: Psoriasis
0.850 GeneticVariation BEFREE We have replicated the association of TRAF3IP2-_rs33980500 variant with the susceptibility to psoriasis. 24005976 2014
Pustular psoriasis
CUI: C0152081
Disease: Pustular psoriasis
0.010 GeneticVariation BEFREE Analyses of clinically relevant phenotypes revealed association of rs33980500 with pustular psoriasis (OR = 1.2, p = 0.0109). 24005976 2014
Psoriasis
CUI: C0033860
Disease: Psoriasis
0.850 GeneticVariation BEFREE By contrast, healthy individuals homozygous for the common variant D10N, located in the ACT1 tumor necrosis factor receptor-associated factor-interacting domain and previously associated with psoriasis, had impaired, but not abolished, responses to IL-17 cytokines. 24120361 2013
Psoriasis
CUI: C0033860
Disease: Psoriasis
0.850 GeneticVariation BEFREE The hyperactive Th17 response combined with fully responsive fibroblasts likely synergized to contribute to psoriasis susceptibility in SNP-D10N patients. 25024377 2014
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
0.010 GeneticVariation BEFREE Lacking this compensatory mechanism, ACT1(D10N/D10N) T cells behave like ACT1-deficient T cells, exhibiting a dysregulated and hyperactive Th17 phenotype with overproduction of IL-22 and IL-17. 25024377 2014
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
0.820 GeneticVariation GWASCAT Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. 26626624 2015
Psoriasis vulgaris
CUI: C0263361
Disease: Psoriasis vulgaris
0.710 GeneticVariation GWASCAT Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. 26626624 2015
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
0.010 GeneticVariation BEFREE T allele of TRAF3IP2 rs33980500 was also associated with female gender, family history of cardiovascular disease, and mechanical complications of heart (P = .04, P = .02, and P = .01, respectively). 29430728 2018
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.010 GeneticVariation BEFREE To compare frequencies of functional polymorphisms of TRAF3IP2 (rs13210247, rs33980500) between patients with MI and healthy controls. 29430728 2018