rs1077667
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1077667(A;A) |
| Make rs1077667(A;G) |
| Make rs1077667(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 6668961 |
| Gene | TNFSF14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1077667 |
| dbSNP (classic) | rs1077667 |
| ClinGen | rs1077667 |
| ebi | rs1077667 |
| HLI | rs1077667 |
| Exac | rs1077667 |
| Gnomad | rs1077667 |
| Varsome | rs1077667 |
| LitVar | rs1077667 |
| Map | rs1077667 |
| PheGenI | rs1077667 |
| Biobank | rs1077667 |
| 1000 genomes | rs1077667 |
| hgdp | rs1077667 |
| ensembl | rs1077667 |
| geneview | rs1077667 |
| scholar | rs1077667 |
| rs1077667 | |
| pharmgkb | rs1077667 |
| gwascentral | rs1077667 |
| openSNP | rs1077667 |
| 23andMe | rs1077667 |
| SNPshot | rs1077667 |
| SNPdbe | rs1077667 |
| MSV3d | rs1077667 |
| GWAS Ctlg | rs1077667 |
| GMAF | 0.2351 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
23andMe blog multiple sclerosis rs1077667 TNFSF14 T 0.88
| GWAS snp | |
|---|---|
| PMID | [PMID 21833088 ]
|
| Trait | |
| Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
| Risk Allele | G |
| P-val | 9E-14 |
| Odds Ratio | 1.1600 [1.14-1.18] |
[PMID 23037546] Serum levels of LIGHT in MS
