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rs2293152

From SNPedia

Orientationminus
Stabilizedminus
Make rs2293152(C;C)
Make rs2293152(C;G)
Make rs2293152(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position42329511
GeneSTAT3
is asnp
is mentioned by
dbSNPrs2293152
ebirs2293152
HLIrs2293152
Exacrs2293152
Varsomers2293152
Maprs2293152
PheGenIrs2293152
hapmaprs2293152
1000 genomesrs2293152
hgdprs2293152
ensemblrs2293152
gopubmedrs2293152
geneviewrs2293152
scholarrs2293152
googlers2293152
pharmgkbrs2293152
gwascentralrs2293152
openSNPrs2293152
23andMers2293152
23andMe allrs2293152
SNP Nexus

SNPshotrs2293152
SNPdbers2293152
MSV3drs2293152
GWAS Ctlgrs2293152
GMAF0.3792
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 19653082OA-icon.png] Strong Evidence of a Combination Polymorphism of the Tyrosine Kinase 2 Gene and the Signal Transducer and Activator of Transcription 3 Gene as a DNA-Based Biomarker for Susceptibility to Crohn's Disease in the Japanese Population


[PMID 19776189] Dietary saturated fat modulates the association between STAT3 polymorphisms and abdominal obesity in adults


[PMID 22205606] JAK2 and STAT3 polymorphisms in a Han Chinese Population with Behcet's disease

GWAS snp
PMID [PMID 22190364OA-icon.png]
Trait
Title Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
Risk Allele C
P-val 4E-8
Odds Ratio 1.2200 None

[PMID 15935090OA-icon.png] Polymorphisms in signal transducer and activator of transcription 3 and lung function in asthma.


[PMID 17636079OA-icon.png] Common STAT3 variants are not associated with obesity or insulin resistance in female twins.


[PMID 18451776] Study of genetic variation in the STAT3 on obesity and insulin resistance in male adults.


[PMID 18520591OA-icon.png] Sequence variants in host cell factor C1 are associated with Meniere's disease.


[PMID 18789715] Genetic variants in STAT3 are associated with nonalcoholic fatty liver disease.


[PMID 20159113OA-icon.png] Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.


[PMID 21068102] Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese.


[PMID 21310444] Mitochondrial DNA copy number is modulated by genetic variation in the signal transducer and activator of transcription 3 (STAT3).


[PMID 22095036] Independent replication of STAT3 association with multiple sclerosis risk in a large German case-control sample.


[PMID 23127549] Influence of the STAT3 genetic variants in the susceptibility to psoriatic arthritis and Behcet's disease


[PMID 23611997] JAK1, but not JAK2 and STAT3, confers susceptibility to Vogt-Koyanagi-Harada (VKH) syndrome in a Han Chinese population


[PMID 24081513OA-icon.png] Association of single-nucleotide polymorphisms in the STAT3 gene with autoimmune thyroid disease in Chinese individuals


[PMID 24781989] Association between STAT3 gene polymorphisms and ulcerative colitis susceptibility: a case-control study in the Chinese Han population


[PMID 24864251OA-icon.png] rs744166 Polymorphism of the STAT3 Gene Is Associated with Risk of Gastric Cancer in a Chinese Population


[PMID 26745093] Single Nucleotide Polymorphisms in STAT3 and STAT4 and Risk of Hepatocellular Carcinoma in Thai Patients with Chronic Hepatitis B.