rs373496
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs373496(C;T) |
| Make rs373496(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 11966306 |
| Gene | TNFRSF17 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs373496 |
| dbSNP (classic) | rs373496 |
| ClinGen | rs373496 |
| ebi | rs373496 |
| HLI | rs373496 |
| Exac | rs373496 |
| Gnomad | rs373496 |
| Varsome | rs373496 |
| LitVar | rs373496 |
| Map | rs373496 |
| PheGenI | rs373496 |
| Biobank | rs373496 |
| 1000 genomes | rs373496 |
| hgdp | rs373496 |
| ensembl | rs373496 |
| geneview | rs373496 |
| scholar | rs373496 |
| rs373496 | |
| pharmgkb | rs373496 |
| gwascentral | rs373496 |
| openSNP | rs373496 |
| 23andMe | rs373496 |
| SNPshot | rs373496 |
| SNPdbe | rs373496 |
| MSV3d | rs373496 |
| GWAS Ctlg | rs373496 |
| GMAF | 0.03765 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 16318629
] On the genetic involvement of apoptosis-related genes in Crohn's disease as revealed by an extended association screen using 245 markers: no evidence for new predisposing factors.
[PMID 18254984] Screening of functional and positional candidate genes in families with common variable immunodeficiency.
