rs2291667
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs2291667(C;T) |
| Make rs2291667(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 6669975 |
| Gene | TNFSF14 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2291667 |
| dbSNP (classic) | rs2291667 |
| ClinGen | rs2291667 |
| ebi | rs2291667 |
| HLI | rs2291667 |
| Exac | rs2291667 |
| Gnomad | rs2291667 |
| Varsome | rs2291667 |
| LitVar | rs2291667 |
| Map | rs2291667 |
| PheGenI | rs2291667 |
| Biobank | rs2291667 |
| 1000 genomes | rs2291667 |
| hgdp | rs2291667 |
| ensembl | rs2291667 |
| geneview | rs2291667 |
| scholar | rs2291667 |
| rs2291667 | |
| pharmgkb | rs2291667 |
| gwascentral | rs2291667 |
| openSNP | rs2291667 |
| 23andMe | rs2291667 |
| SNPshot | rs2291667 |
| SNPdbe | rs2291667 |
| MSV3d | rs2291667 |
| GWAS Ctlg | rs2291667 |
| GMAF | 0.003673 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20592286
] Polymorphic Variants of LIGHT (TNF Superfamily-14) Alter Receptor Avidity and Bioavailability
