rs2293152
| Orientation | minus |
| Stabilized | minus |
| Make rs2293152(C;C) |
| Make rs2293152(C;G) |
| Make rs2293152(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 42329511 |
| Gene | STAT3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2293152 |
| dbSNP (classic) | rs2293152 |
| ClinGen | rs2293152 |
| ebi | rs2293152 |
| HLI | rs2293152 |
| Exac | rs2293152 |
| Gnomad | rs2293152 |
| Varsome | rs2293152 |
| LitVar | rs2293152 |
| Map | rs2293152 |
| PheGenI | rs2293152 |
| Biobank | rs2293152 |
| 1000 genomes | rs2293152 |
| hgdp | rs2293152 |
| ensembl | rs2293152 |
| geneview | rs2293152 |
| scholar | rs2293152 |
| rs2293152 | |
| pharmgkb | rs2293152 |
| gwascentral | rs2293152 |
| openSNP | rs2293152 |
| 23andMe | rs2293152 |
| SNPshot | rs2293152 |
| SNPdbe | rs2293152 |
| MSV3d | rs2293152 |
| GWAS Ctlg | rs2293152 |
| GMAF | 0.3792 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19653082
] 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 22190364]
|
| 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 15935090] Polymorphisms in signal transducer and activator of transcription 3 and lung function in asthma.
[PMID 17636079] 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 18520591] 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 20159113] 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 24081513] 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 24864251] 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.
[PMID 29853721] Lack of significant association between selected STAT3 polymorphisms and rheumatoid arthritis in the Polish population.
[PMID 31114439] Ankylosing spondylitis: analysis of gene-gene interactions between IL-12β, JAK2, and STAT3 in Han Chinese and Algerian cohorts.
