rs6478106
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6478106(C;C) |
| Make rs6478106(C;T) |
| Make rs6478106(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 114783386 |
| Gene | TNFSF15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6478106 |
| dbSNP (classic) | rs6478106 |
| ClinGen | rs6478106 |
| ebi | rs6478106 |
| HLI | rs6478106 |
| Exac | rs6478106 |
| Gnomad | rs6478106 |
| Varsome | rs6478106 |
| LitVar | rs6478106 |
| Map | rs6478106 |
| PheGenI | rs6478106 |
| Biobank | rs6478106 |
| 1000 genomes | rs6478106 |
| hgdp | rs6478106 |
| ensembl | rs6478106 |
| geneview | rs6478106 |
| scholar | rs6478106 |
| rs6478106 | |
| pharmgkb | rs6478106 |
| gwascentral | rs6478106 |
| openSNP | rs6478106 |
| 23andMe | rs6478106 |
| SNPshot | rs6478106 |
| SNPdbe | rs6478106 |
| MSV3d | rs6478106 |
| GWAS Ctlg | rs6478106 |
| GMAF | 0.36 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23266558] |
| Trait | Crohn's disease |
| Title | A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population. |
| Risk Allele | T |
| P-val | 5E-46 |
| Odds Ratio | 1.73 [1.60-1.86] |
[PMID 27647972
] A case-control study about the association between vascular endothelial growth inhibitor gene polymorphisms and breast cancer risk in female patients in Northeast China.
[PMID 31844038] Polymorphisms of the TNF Gene and Three Susceptibility Loci Are Associated with Crohn's Disease and Perianal Fistula Crohn's Disease: A Study among the Han Population from South China.
[PMID 33287909] The haplotypes of various TNF related genes associated with scleritis in Chinese Han.
