TRIM26, tripartite motif containing 26, 7726

N. diseases: 31; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2021722
rs2021722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.800 GeneticVariation GWASDB Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs2021722
rs2021722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0036341
Disease:
Schizophrenia 		0.800 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs2021722
rs2021722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.800 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs2523722
rs2523722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0036341
Disease:
Schizophrenia 		0.800 GeneticVariation GWASDB Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate. 23637625 2013
dbSNP: rs2523722
rs2523722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0036341
Disease:
Schizophrenia 		G 0.800 GeneticVariation GWASDB Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia. 22883433 2012
dbSNP: rs2523722
rs2523722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0036341
Disease:
Schizophrenia 		G 0.800 GeneticVariation GWASCAT Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia. 22883433 2012
dbSNP: rs2021722
rs2021722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0036341
Disease:
Schizophrenia 		C 0.800 GeneticVariation GWASDB Genome-wide association study identifies five new schizophrenia loci. 21926974 2011
dbSNP: rs2021722
rs2021722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0036341
Disease:
Schizophrenia 		C 0.800 GeneticVariation GWASCAT Genome-wide association study identifies five new schizophrenia loci. 21926974 2011
dbSNP: rs1117490
rs1117490
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0264408
Disease:
Childhood asthma 		C 0.700 GeneticVariation GWASCAT Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. 31036433 2019
dbSNP: rs1117490
rs1117490
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0741260
Disease:
Adult onset asthma 		C 0.700 GeneticVariation GWASCAT Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. 31036433 2019
dbSNP: rs114265779
rs114265779
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0003872
Disease:
Arthritis, Psoriatic 		0.700 GeneticVariation GWASCAT Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis. 30552173 2019
dbSNP: rs116408368
rs116408368
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
dbSNP: rs116408368
rs116408368
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		T 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs116408368
rs116408368
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0036341
Disease:
Schizophrenia 		T 0.700 GeneticVariation GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
dbSNP: rs116418332
rs116418332
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0149782
Disease:
Squamous cell carcinoma of lung 		A 0.700 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730 2017
dbSNP: rs116418332
rs116418332
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0684249
Disease:
Carcinoma of lung 		A 0.700 GeneticVariation GWASCAT Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. 28604730 2017
dbSNP: rs2844775
rs2844775
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0001807
Disease:
Aggressive behavior 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of proneness to anger. 24489884 2014
dbSNP: rs2844775
rs2844775
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0002957
Disease:
Anger 		A 0.700 GeneticVariation GWASDB Genome-wide association study of proneness to anger. 24489884 2014
dbSNP: rs2021722
rs2021722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C1269683
Disease:
Major Depressive Disorder 		0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs2021722
rs2021722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0005586
Disease:
Bipolar Disorder 		0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs2021722
rs2021722
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013
dbSNP: rs11967808
rs11967808
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C0042900
Disease:
Vitiligo 		0.700 GeneticVariation GWASDB Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. 20526339 2010
dbSNP: rs2072107
rs2072107
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs2072107
rs2072107
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010
dbSNP: rs2072107
rs2072107
Entrez Id: 7726
Gene Symbol: TRIM26
TRIM26
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 GeneticVariation GWASDB The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. 21051598 2010