TNFAIP3, TNF alpha induced protein 3, 7128

N. diseases: 212; N. variants: 29
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs864321625
rs864321625
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C4225218
Disease:
AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE
A 0.700 CausalMutation CLINVAR
dbSNP: rs864321626
rs864321626
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C4225218
Disease:
AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE
T 0.700 CausalMutation CLINVAR
dbSNP: rs864321682
rs864321682
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C4225218
Disease:
AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE
A 0.700 CausalMutation CLINVAR
dbSNP: rs864321683
rs864321683
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C4225218
Disease:
AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE
C 0.700 CausalMutation CLINVAR
dbSNP: rs864321684
rs864321684
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C4225218
Disease:
AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE
G 0.700 CausalMutation CLINVAR
dbSNP: rs864321685
rs864321685
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C4225218
Disease:
AUTOINFLAMMATORY SYNDROME, FAMILIAL, BEHCET-LIKE
T 0.700 CausalMutation CLINVAR
dbSNP: rs5029930
rs5029930
Entrez Id: 7128;100130476
Gene Symbol: TNFAIP3;WAKMAR2
TNFAIP3;WAKMAR2
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE Two tag SNPs (rs5029930 and rs610604) were independently associated with CAD; adjusted odds ratios (ORs) for minor allele carriers were 2.3 (95% CI 1.4-3.8, P = 0.001) and 2.0 (1.3-2.9, P = 0.0008), respectively. 17259397 2007
dbSNP: rs610604
rs610604
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE Two tag SNPs (rs5029930 and rs610604) were independently associated with CAD; adjusted odds ratios (ORs) for minor allele carriers were 2.3 (95% CI 1.4-3.8, P = 0.001) and 2.0 (1.3-2.9, P = 0.0008), respectively. 17259397 2007
dbSNP: rs2230926
rs2230926
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.900 GeneticVariation BEFREE We show that three independent SNPs in the TNFAIP3 region (rs13192841, rs2230926 and rs6922466) are associated with systemic lupus erythematosus (SLE) among individuals of European ancestry. 19165919 2008
dbSNP: rs5029939
rs5029939
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.850 GeneticVariation BEFREE We carried out a genome-wide association scan and replication study and found an association between SLE and a variant in TNFAIP3 (rs5029939, meta-analysis P = 2.89 x 10(-12), OR = 2.29). 19165918 2008
dbSNP: rs5029939
rs5029939
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.850 GeneticVariation GWASCAT We carried out a genome-wide association scan and replication study and found an association between SLE and a variant in TNFAIP3 (rs5029939, meta-analysis P = 2.89 x 10(-12), OR = 2.29). 19165918 2008
dbSNP: rs5029939
rs5029939
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.850 GeneticVariation GWASDB We carried out a genome-wide association scan and replication study and found an association between SLE and a variant in TNFAIP3 (rs5029939, meta-analysis P = 2.89 x 10(-12), OR = 2.29). 19165918 2008
dbSNP: rs2230926
rs2230926
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
C 0.900 GeneticVariation GWASCAT Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. 19838193 2009
dbSNP: rs2230926
rs2230926
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
C 0.900 GeneticVariation GWASDB Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. 19838193 2009
dbSNP: rs610604
rs610604
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0033860
Disease:
Psoriasis
G 0.860 GeneticVariation GWASDB Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. 19169254 2009
dbSNP: rs610604
rs610604
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0033860
Disease:
Psoriasis
G 0.860 GeneticVariation GWASCAT Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. 19169254 2009
dbSNP: rs5029937
rs5029937
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.740 GeneticVariation BEFREE The combination of the carriage of both risk alleles of rs6920220 and rs5029937 together with the absence of the protective allele of rs13207033 was strongly associated with RA when compared with carriage of none [OR of 1.86 (95% CI) (1.51-2.29)]. 19417005 2009
dbSNP: rs5029937
rs5029937
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
T 0.710 GeneticVariation GWASCAT A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus. 19838195 2009
dbSNP: rs582757
rs582757
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.020 GeneticVariation BEFREE The rs582757 SNP and a common haplotype in the TNFAIP3 locus exhibited association with RA. 19292917 2009
dbSNP: rs582757
rs582757
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0035439
Disease:
Rheumatic Heart Disease
0.010 GeneticVariation BEFREE Therefore, we report a new genetic variant (rs582757) in the TNFAIP3 gene that associated with the prevalence of RHD in Chinese Han population. 19902201 2009
dbSNP: rs2230926
rs2230926
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.900 GeneticVariation BEFREE We observed a significant association between rs2230926 and an increased risk of SLE and RA in the Japanese population (for SLE, odds ratio [OR] 1.92, 95% confidence interval [95% CI] 1.53-2.41, P = 1.9 x 10(-8); for RA, OR 1.35, 95% CI 1.18-1.56, P = 2.6 x 10(-5)). 20112363 2010
dbSNP: rs2230926
rs2230926
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.900 GeneticVariation BEFREE There are two nonsynonymous coding polymorphisms in the deubiquitinating (DUB) domain of TNFAIP3: F127C, which is in high-linkage disequilibrium with reported SLE-risk variants, and A125V, which has not been previously studied. 20483768 2010
dbSNP: rs2230926
rs2230926
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.900 GeneticVariation BEFREE Our findings suggest that SNP rs2230926 in the TNFAIP3 might be a common genetic factor for SLE within different populations in terms of Chinese Han and European population. 19774492 2010
dbSNP: rs610604
rs610604
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0033860
Disease:
Psoriasis
0.860 GeneticVariation GWASDB Association analyses identify six new psoriasis susceptibility loci in the Chinese population. 20953187 2010
dbSNP: rs610604
rs610604
Entrez Id: 7128
Gene Symbol: TNFAIP3
TNFAIP3
CUI: C0033860
Disease:
Psoriasis
0.860 GeneticVariation GWASCAT A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. 20953190 2010