rs3861950
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3861950(C;C) |
| Make rs3861950(C;T) |
| Make rs3861950(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 1 |
| Position | 173187153 |
| Gene | TNFSF4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3861950 |
| dbSNP (classic) | rs3861950 |
| ClinGen | rs3861950 |
| ebi | rs3861950 |
| HLI | rs3861950 |
| Exac | rs3861950 |
| Gnomad | rs3861950 |
| Varsome | rs3861950 |
| LitVar | rs3861950 |
| Map | rs3861950 |
| PheGenI | rs3861950 |
| Biobank | rs3861950 |
| 1000 genomes | rs3861950 |
| hgdp | rs3861950 |
| ensembl | rs3861950 |
| geneview | rs3861950 |
| scholar | rs3861950 |
| rs3861950 | |
| pharmgkb | rs3861950 |
| gwascentral | rs3861950 |
| openSNP | rs3861950 |
| 23andMe | rs3861950 |
| SNPshot | rs3861950 |
| SNPdbe | rs3861950 |
| MSV3d | rs3861950 |
| GWAS Ctlg | rs3861950 |
| GMAF | 0.3898 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 21402531] [Association study between TNFSF4 and coronary heart disease]
[PMID 21445270
] A common polymorphism in the promoter region of the TNFSF4 gene is associated with lower allele-specific expression and risk of myocardial infarction.
[PMID 23184501] TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese population
[PMID 26814870] [Association between tumor necrosis factor superfamily member 4 gene polymorphism and risk of asymptomatic carotid vulnerable plaque in a Chinese population].
[PMID 33329013] A Meta-Analysis on the Association Between TNFSF4 Polymorphisms (rs3861950 T > C and rs1234313 A > G) and Susceptibility to Coronary Artery Disease.
