rs13238568
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
Red cell distribution width determination
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs13238568
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
RDW - Red blood cell distribution width result
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs2527366
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
Body mass index
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs36044436
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
Blood Pressure
0.700
GeneticVariation
GWASCAT
Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis.
30940143
2019
rs36044436
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
Chronic Obstructive Airway Disease
0.700
GeneticVariation
GWASCAT
Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis.
30940143
2019
rs6964833
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
Age at menarche
T
0.700
GeneticVariation
GWASCAT
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.
25231870
2014
rs7794284
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
Cardiovascular Diseases
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs13227433
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
Social Anxiety
0.010
GeneticVariation
BEFREE
The GTF2I rs13227433 AA genotype, previously associated with lower social anxiety , predicted decreased threat-related amygdala reactivity.
26853120
2017
rs2527367
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
Anxiety neurosis (finding)
0.010
GeneticVariation
BEFREE
Because of this recent preclinical and clinical identification of a genetic influence on anxiety, we examined whether sequence variation in GTF2I, specifically the single-nucleotide polymorphism rs2527367 , interacts with trait and state anxiety to collectively impact neural response to anxiety-laden social stimuli.
26285132
2015
rs2527367
×
Entrez Id:
2969
Gene Symbol:
GTF2I
GTF2I
Anxiety state
0.010
GeneticVariation
BEFREE
Because of this recent preclinical and clinical identification of a genetic influence on anxiety, we examined whether sequence variation in GTF2I, specifically the single-nucleotide polymorphism rs2527367 , interacts with trait and state anxiety to collectively impact neural response to anxiety-laden social stimuli.
26285132
2015
rs117026326
GTF2I;LOC101926943
Sjogren's Syndrome
T
0.800
GeneticVariation
GWASCAT
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23.
24097066
2013
rs117026326
GTF2I;LOC101926943
Sjogren's Syndrome
T
0.800
GeneticVariation
GWASDB
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23.
24097066
2013
rs117026326
GTF2I;LOC101926943
Sjogren's Syndrome
T
0.800
GeneticVariation
GWASCAT
Identification of susceptibility gene associated with female primary Sjögren's syndrome in Han Chinese by genome-wide association study.
27503288
2016
rs2465936
GTF2I;LOC101926943
mathematical ability
G
0.700
GeneticVariation
GWASCAT
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
30038396
2018
rs2718277
GTF2I;LOC101926943
mathematical ability
T
0.700
GeneticVariation
GWASCAT
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.
30038396
2018
rs34324971
GTF2I;LOC101926943
Diastolic blood pressure
A
0.700
GeneticVariation
GWASCAT
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
30224653
2018
rs35005436
GTF2I;LOC101926943
Atrial Fibrillation
C
0.700
GeneticVariation
GWASCAT
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
30061737
2018
rs35005436
GTF2I;LOC101926943
Age at menarche
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs74910854
GTF2I;LOC101926943
Atrial Fibrillation
G
0.700
GeneticVariation
GWASCAT
Multi-ethnic genome-wide association study for atrial fibrillation.
29892015
2018
rs7795281
GTF2I;LOC101926943
C-reactive protein measurement
A
0.700
GeneticVariation
GWASCAT
Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.
30388399
2018
rs117026326
GTF2I;LOC101926943
Lupus Erythematosus, Systemic
0.040
GeneticVariation
BEFREE
This study demonstrates a significant association between SLE and the GTF2I rs117026326 T allele, GTF2IRD1 rs4717901 C allele.
26320362
2015
rs117026326
GTF2I;LOC101926943
Lupus Erythematosus, Systemic
0.040
GeneticVariation
BEFREE
Genetic variant rs117026326 upstream of the general transcription factor II-I (GTF2I) has been associated with primary Sjögren's syndrome, SLE and RA in East Asian populations.
31520790
2019
rs117026326
GTF2I;LOC101926943
Lupus Erythematosus, Systemic
0.040
GeneticVariation
BEFREE
The relationship between gene polymorphism of rs117026326 , rs73366469, and susceptibility, progression of SLE were analyzed.The present study provided evidence that rs117026326 and rs73366469 were both associated with SLE susceptibility (both C vs T: P < .001).
31374066
2019
rs117026326
GTF2I;LOC101926943
Lupus Erythematosus, Systemic
0.040
GeneticVariation
BEFREE
Genome-wide association studies of systemic lupus erythematosus (SLE ) in Chinese and Korean populations demonstrated strong association of single nucleotide polymorphisms (SNPs) located in the GTF2I-NCF1 region, rs73366469 (GTF2I), rs117026326 (GTF2I), rs80346167(GTF2IRD1) and rs201802880 (NCF1).
31705128
2019
rs117026326
GTF2I;LOC101926943
Primary Sjögren's syndrome
0.020
GeneticVariation
BEFREE
The combined analysis identified GTF2I at 7q11.23 (rs117026326 : Pcombined = 1.31 × 10(-53), combined odds ratio (ORcombined) = 2.20) as a new susceptibility locus for primary Sjögren's syndrome .
24097066
2013